rs757154921

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Species

Homo sapiens

Symbol

rs757154921

Category

Variant

Variant type

SNP

Overlaps

MYL6

Location

12:56158684

Nucleotide Change

T>C

Most Severe Consequence

• splice region variant&non coding transcript exon variant

See all consequences

HGVS.g name

• NC_000012.12:g.56158684T>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000293422.9:c.7T>C
• ENSEMBL:ENST00000348108.8:c.7T>C

Show All 21

HGVS.p name

• ENSP00000293422:p.Cys3Arg
• ENSP00000301540:p.Cys3Arg

Show All 13

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences