rs760739044

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Species

Homo sapiens

Symbol

rs760739044

Category

Variant

Variant type

SNP

Overlaps

ABCA12

Location

2:214959092

Nucleotide Change

C>G

Most Severe Consequence

• intron variant&non coding transcript variant

See all consequences

HGVS.g name

• (GRCh38)2:214959092C>G

Show All 5

HGVS.c name

• ENSEMBL:ENST00000272895.12:c.5885-14G>C
• ENSEMBL:ENST00000389661.4:c.4931-14G>C

Show All 16

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences