Canonical Allele Identifier: CA64803958

Gene: ABCA12

Linked Data

• dbSNP Id: rs769092601
• gnomAD v2: 2-215884516-G-T
• gnomAD v4: 2-215019792-G-T
• MyVariant Identifiers: chr2:g.215884516G>T (hg19) ; chr2:g.215019792G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215019792G>T , CM000664.2:g.215019792G>T	GRCh38
NC_000002.11:g.215884516G>T , CM000664.1:g.215884516G>T	GRCh37
NC_000002.10:g.215592761G>T	NCBI36
NG_007074.1:g.123636C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.1292C>A MANE Select	ENSP00000272895.7:p.Ser431Tyr
ENST00000272895.11:c.1292C>A	ENSP00000272895.7:p.Ser431Tyr
ENST00000389661.4:c.338C>A	ENSP00000374312.4:p.Ser113Tyr
NM_015657.3:c.338C>A	NP_056472.2:p.Ser113Tyr
NM_173076.2:c.1292C>A	NP_775099.2:p.Ser431Tyr
NR_103740.1:n.1536C>A
XM_011510951.1:c.1292C>A	XP_011509253.1:p.Ser431Tyr
XM_011510952.1:c.1292C>A	XP_011509254.1:p.Ser431Tyr
XM_011510951.2:c.1292C>A	XP_011509253.1:p.Ser431Tyr
NM_173076.3:c.1292C>A MANE Select	NP_775099.2:p.Ser431Tyr
NR_103740.2:n.1734C>A
NM_015657.4:c.338C>A	NP_056472.2:p.Ser113Tyr