Canonical Allele Identifier: CA431319342
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215809748A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214945024A>G , CM000664.2:g.214945024A>G GRCh38
NC_000002.11:g.215809748A>G , CM000664.1:g.215809748A>G GRCh37
NC_000002.10:g.215517993A>G NCBI36
NG_007074.1:g.198404T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.7320T>C (ABCA12) MANE Select ENSP00000272895.7:p.Cys2440=
ENST00000272895.11:c.7320T>C (ABCA12) ENSP00000272895.7:p.Cys2440=
ENST00000389661.4:c.6366T>C (ABCA12) ENSP00000374312.4:p.Cys2122=
NM_015657.3:c.6366T>C (ABCA12) NP_056472.2:p.Cys2122=
NM_173076.2:c.7320T>C (ABCA12) NP_775099.2:p.Cys2440=
NR_103740.1:n.7620T>C (ABCA12)
NR_110292.1:n.322-2801A>G (SNHG31)
XM_011510951.1:c.7329T>C (ABCA12) XP_011509253.1:p.Cys2443=
XM_011510951.2:c.7329T>C (ABCA12) XP_011509253.1:p.Cys2443=
NM_173076.3:c.7320T>C (ABCA12) MANE Select NP_775099.2:p.Cys2440=
NR_103740.2:n.7818T>C (ABCA12)
NM_015657.4:c.6366T>C (ABCA12) NP_056472.2:p.Cys2122=