Canonical Allele Identifier: CA2662973806

Gene: ABCA12 SNHG31

Linked Data

• gnomAD v4: 2-214932072-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932072T>C , CM000664.2:g.214932072T>C	GRCh38
NC_000002.11:g.215796796T>C , CM000664.1:g.215796796T>C	GRCh37
NC_000002.10:g.215505041T>C	NCBI36
NG_007074.1:g.211356A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.*562A>G (ABCA12) MANE Select	ENSP00000272895.7:n.*562A>G
ENST00000272895.11:c.*562A>G (ABCA12)	ENSP00000272895.7:n.*562A>G
NM_015657.3:c.*562A>G (ABCA12)	NP_056472.2:n.*562A>G
NM_173076.2:c.*562A>G (ABCA12)	NP_775099.2:n.*562A>G
NR_103740.1:n.8650A>G (ABCA12)
NR_110292.1:n.322-15753T>C (SNHG31)
XM_011510951.1:c.*562A>G (ABCA12)	XP_011509253.1:n.*562A>G
XM_011510951.2:c.*562A>G (ABCA12)	XP_011509253.1:n.*562A>G
NM_173076.3:c.*562A>G (ABCA12) MANE Select	NP_775099.2:n.*562A>G
NR_103740.2:n.8848A>G (ABCA12)
NM_015657.4:c.*562A>G (ABCA12)	NP_056472.2:n.*562A>G