Canonical Allele Identifier: CA431319347
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215809760T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214945036T>C , CM000664.2:g.214945036T>C GRCh38
NC_000002.11:g.215809760T>C , CM000664.1:g.215809760T>C GRCh37
NC_000002.10:g.215518005T>C NCBI36
NG_007074.1:g.198392A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.7308A>G (ABCA12) MANE Select ENSP00000272895.7:p.Val2436=
ENST00000272895.11:c.7308A>G (ABCA12) ENSP00000272895.7:p.Val2436=
ENST00000389661.4:c.6354A>G (ABCA12) ENSP00000374312.4:p.Val2118=
NM_015657.3:c.6354A>G (ABCA12) NP_056472.2:p.Val2118=
NM_173076.2:c.7308A>G (ABCA12) NP_775099.2:p.Val2436=
NR_103740.1:n.7608A>G (ABCA12)
NR_110292.1:n.322-2789T>C (SNHG31)
XM_011510951.1:c.7317A>G (ABCA12) XP_011509253.1:p.Val2439=
XM_011510951.2:c.7317A>G (ABCA12) XP_011509253.1:p.Val2439=
NM_173076.3:c.7308A>G (ABCA12) MANE Select NP_775099.2:p.Val2436=
NR_103740.2:n.7806A>G (ABCA12)
NM_015657.4:c.6354A>G (ABCA12) NP_056472.2:p.Val2118=