Canonical Allele Identifier: CA350483457

Gene: ABCA12

Linked Data

• gnomAD v4: 2-215011474-T-C
• MyVariant Identifiers: chr2:g.215876198T>C (hg19) ; chr2:g.215011474T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215011474T>C , CM000664.2:g.215011474T>C	GRCh38
NC_000002.11:g.215876198T>C , CM000664.1:g.215876198T>C	GRCh37
NC_000002.10:g.215584443T>C	NCBI36
NG_007074.1:g.131954A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.2297A>G MANE Select	ENSP00000272895.7:p.Gln766Arg
ENST00000272895.11:c.2297A>G	ENSP00000272895.7:p.Gln766Arg
ENST00000389661.4:c.1343A>G	ENSP00000374312.4:p.Gln448Arg
NM_015657.3:c.1343A>G	NP_056472.2:p.Gln448Arg
NM_173076.2:c.2297A>G	NP_775099.2:p.Gln766Arg
NR_103740.1:n.2541A>G
XM_011510951.1:c.2297A>G	XP_011509253.1:p.Gln766Arg
XM_011510952.1:c.2297A>G	XP_011509254.1:p.Gln766Arg
XM_011510951.2:c.2297A>G	XP_011509253.1:p.Gln766Arg
NM_173076.3:c.2297A>G MANE Select	NP_775099.2:p.Gln766Arg
NR_103740.2:n.2739A>G
NM_015657.4:c.1343A>G	NP_056472.2:p.Gln448Arg