Canonical Allele Identifier: CA350793964

Gene: ABCA12 SNHG31

Linked Data

• dbSNP Id: rs1698619412
• MyVariant Identifiers: chr2:g.215812225G>T (hg19) ; chr2:g.214947501G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214947501G>T , CM000664.2:g.214947501G>T	GRCh38
NC_000002.11:g.215812225G>T , CM000664.1:g.215812225G>T	GRCh37
NC_000002.10:g.215520470G>T	NCBI36
NG_007074.1:g.195927C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.7160C>A (ABCA12) MANE Select	ENSP00000272895.7:p.Thr2387Asn
ENST00000272895.11:c.7160C>A (ABCA12)	ENSP00000272895.7:p.Thr2387Asn
ENST00000389661.4:c.6206C>A (ABCA12)	ENSP00000374312.4:p.Thr2069Asn
NM_015657.3:c.6206C>A (ABCA12)	NP_056472.2:p.Thr2069Asn
NM_173076.2:c.7160C>A (ABCA12)	NP_775099.2:p.Thr2387Asn
NR_103740.1:n.7460C>A (ABCA12)
NR_110292.1:n.322-324G>T (SNHG31)
XM_011510951.1:c.7169C>A (ABCA12)	XP_011509253.1:p.Thr2390Asn
XM_011510951.2:c.7169C>A (ABCA12)	XP_011509253.1:p.Thr2390Asn
NM_173076.3:c.7160C>A (ABCA12) MANE Select	NP_775099.2:p.Thr2387Asn
NR_103740.2:n.7658C>A (ABCA12)
NM_015657.4:c.6206C>A (ABCA12)	NP_056472.2:p.Thr2069Asn