Canonical Allele Identifier: CA431319061

Gene: ABCA12 SNHG31

Linked Data

• MyVariant Identifiers: chr2:g.215797424A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214932700A>T , CM000664.2:g.214932700A>T	GRCh38
NC_000002.11:g.215797424A>T , CM000664.1:g.215797424A>T	GRCh37
NC_000002.10:g.215505669A>T	NCBI36
NG_007074.1:g.210728T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272895.12:c.7722T>A (ABCA12) MANE Select	ENSP00000272895.7:p.Thr2574=
ENST00000272895.11:c.7722T>A (ABCA12)	ENSP00000272895.7:p.Thr2574=
ENST00000389661.4:c.6768T>A (ABCA12)	ENSP00000374312.4:p.Thr2256=
NM_015657.3:c.6768T>A (ABCA12)	NP_056472.2:p.Thr2256=
NM_173076.2:c.7722T>A (ABCA12)	NP_775099.2:p.Thr2574=
NR_103740.1:n.8022T>A (ABCA12)
NR_110292.1:n.322-15125A>T (SNHG31)
XM_011510951.1:c.7731T>A (ABCA12)	XP_011509253.1:p.Thr2577=
XM_011510951.2:c.7731T>A (ABCA12)	XP_011509253.1:p.Thr2577=
NM_173076.3:c.7722T>A (ABCA12) MANE Select	NP_775099.2:p.Thr2574=
NR_103740.2:n.8220T>A (ABCA12)
NM_015657.4:c.6768T>A (ABCA12)	NP_056472.2:p.Thr2256=