rs780321086

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Species

Homo sapiens

Symbol

rs780321086

Category

Variant

Variant type

SNP

Overlaps

RBKS

Location

2:27847066

Nucleotide Change

C>A

Most Severe Consequence

• intron variant&non coding transcript variant

See all consequences

HGVS.g name

• NC_000002.12:g.27847066C>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000302188.8:c.325G>T
• ENSEMBL:ENST00000448427.1:n.204-47467C>A

Show All 3

HGVS.p name

• ENSP00000306817:p.Ala109Ser

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences