Canonical Allele Identifier: CA65501405

Gene: ABCA12 SNHG31

Linked Data

• dbSNP Id: rs967355477
• MyVariant Identifiers: chr2:g.215797198T>A (hg19) ; chr2:g.214932474T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932474T>A , CM000664.2:g.214932474T>A	GRCh38
NC_000002.11:g.215797198T>A , CM000664.1:g.215797198T>A	GRCh37
NC_000002.10:g.215505443T>A	NCBI36
NG_007074.1:g.210954A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.*160A>T (ABCA12) MANE Select	ENSP00000272895.7:n.*160A>T
ENST00000272895.11:c.*160A>T (ABCA12)	ENSP00000272895.7:n.*160A>T
NM_015657.3:c.*160A>T (ABCA12)	NP_056472.2:n.*160A>T
NM_173076.2:c.*160A>T (ABCA12)	NP_775099.2:n.*160A>T
NR_103740.1:n.8248A>T (ABCA12)
NR_110292.1:n.322-15351T>A (SNHG31)
XM_011510951.1:c.*160A>T (ABCA12)	XP_011509253.1:n.*160A>T
XM_011510951.2:c.*160A>T (ABCA12)	XP_011509253.1:n.*160A>T
NM_173076.3:c.*160A>T (ABCA12) MANE Select	NP_775099.2:n.*160A>T
NR_103740.2:n.8446A>T (ABCA12)
NM_015657.4:c.*160A>T (ABCA12)	NP_056472.2:n.*160A>T