Canonical Allele Identifier: CA1327140536

Gene: ABCA12 SNHG31

Linked Data

• dbSNP Id: rs1698075463

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932074A>C , CM000664.2:g.214932074A>C	GRCh38
NC_000002.11:g.215796798A>C , CM000664.1:g.215796798A>C	GRCh37
NC_000002.10:g.215505043A>C	NCBI36
NG_007074.1:g.211354T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.*560T>G (ABCA12) MANE Select	ENSP00000272895.7:n.*560T>G
ENST00000272895.11:c.*560T>G (ABCA12)	ENSP00000272895.7:n.*560T>G
NM_015657.3:c.*560T>G (ABCA12)	NP_056472.2:n.*560T>G
NM_173076.2:c.*560T>G (ABCA12)	NP_775099.2:n.*560T>G
NR_103740.1:n.8648T>G (ABCA12)
NR_110292.1:n.322-15751A>C (SNHG31)
XM_011510951.1:c.*560T>G (ABCA12)	XP_011509253.1:n.*560T>G
XM_011510951.2:c.*560T>G (ABCA12)	XP_011509253.1:n.*560T>G
NM_173076.3:c.*560T>G (ABCA12) MANE Select	NP_775099.2:n.*560T>G
NR_103740.2:n.8846T>G (ABCA12)
NM_015657.4:c.*560T>G (ABCA12)	NP_056472.2:n.*560T>G