Canonical Allele Identifier: CA350793952

Gene: ABCA12 SNHG31

Linked Data

• MyVariant Identifiers: chr2:g.215812219A>G (hg19) ; chr2:g.214947495A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214947495A>G , CM000664.2:g.214947495A>G	GRCh38
NC_000002.11:g.215812219A>G , CM000664.1:g.215812219A>G	GRCh37
NC_000002.10:g.215520464A>G	NCBI36
NG_007074.1:g.195933T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.7166T>C (ABCA12) MANE Select	ENSP00000272895.7:p.Met2389Thr
ENST00000272895.11:c.7166T>C (ABCA12)	ENSP00000272895.7:p.Met2389Thr
ENST00000389661.4:c.6212T>C (ABCA12)	ENSP00000374312.4:p.Met2071Thr
NM_015657.3:c.6212T>C (ABCA12)	NP_056472.2:p.Met2071Thr
NM_173076.2:c.7166T>C (ABCA12)	NP_775099.2:p.Met2389Thr
NR_103740.1:n.7466T>C (ABCA12)
NR_110292.1:n.322-330A>G (SNHG31)
XM_011510951.1:c.7175T>C (ABCA12)	XP_011509253.1:p.Met2392Thr
XM_011510951.2:c.7175T>C (ABCA12)	XP_011509253.1:p.Met2392Thr
NM_173076.3:c.7166T>C (ABCA12) MANE Select	NP_775099.2:p.Met2389Thr
NR_103740.2:n.7664T>C (ABCA12)
NM_015657.4:c.6212T>C (ABCA12)	NP_056472.2:p.Met2071Thr