Canonical Allele Identifier: CA431148693

Gene: ABCA12

Linked Data

• dbSNP Id: rs1460189984
• gnomAD v3: 2-214980525-T-C
• gnomAD v4: 2-214980525-T-C
• MyVariant Identifiers: chr2:g.215845249T>C (hg19) ; chr2:g.214980525T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214980525T>C , CM000664.2:g.214980525T>C	GRCh38
NC_000002.11:g.215845249T>C , CM000664.1:g.215845249T>C	GRCh37
NC_000002.10:g.215553494T>C	NCBI36
NG_007074.1:g.162903A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.4698A>G MANE Select	ENSP00000272895.7:p.Glu1566=
ENST00000272895.11:c.4698A>G	ENSP00000272895.7:p.Glu1566=
ENST00000389661.4:c.3744A>G	ENSP00000374312.4:p.Glu1248=
NM_015657.3:c.3744A>G	NP_056472.2:p.Glu1248=
NM_173076.2:c.4698A>G	NP_775099.2:p.Glu1566=
NR_103740.1:n.4998A>G
XM_011510951.1:c.4707A>G	XP_011509253.1:p.Glu1569=
XM_011510952.1:c.4707A>G	XP_011509254.1:p.Glu1569=
XM_011510951.2:c.4707A>G	XP_011509253.1:p.Glu1569=
NM_173076.3:c.4698A>G MANE Select	NP_775099.2:p.Glu1566=
NR_103740.2:n.5196A>G
NM_015657.4:c.3744A>G	NP_056472.2:p.Glu1248=