Canonical Allele Identifier: CA431388006

Gene: ABCA12 SNHG31

Linked Data

• MyVariant Identifiers: chr2:g.215818631G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214953907G>T , CM000664.2:g.214953907G>T	GRCh38
NC_000002.11:g.215818631G>T , CM000664.1:g.215818631G>T	GRCh37
NC_000002.10:g.215526876G>T	NCBI36
NG_007074.1:g.189521C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.6594C>A (ABCA12) MANE Select	ENSP00000272895.7:p.Thr2198=
ENST00000272895.11:c.6594C>A (ABCA12)	ENSP00000272895.7:p.Thr2198=
ENST00000389661.4:c.5640C>A (ABCA12)	ENSP00000374312.4:p.Thr1880=
NM_015657.3:c.5640C>A (ABCA12)	NP_056472.2:p.Thr1880=
NM_173076.2:c.6594C>A (ABCA12)	NP_775099.2:p.Thr2198=
NR_103740.1:n.6894C>A (ABCA12)
NR_110292.1:n.444+5960G>T (SNHG31)
XM_011510951.1:c.6603C>A (ABCA12)	XP_011509253.1:p.Thr2201=
XM_011510951.2:c.6603C>A (ABCA12)	XP_011509253.1:p.Thr2201=
NM_173076.3:c.6594C>A (ABCA12) MANE Select	NP_775099.2:p.Thr2198=
NR_103740.2:n.7092C>A (ABCA12)
NM_015657.4:c.5640C>A (ABCA12)	NP_056472.2:p.Thr1880=