Canonical Allele Identifier: CA431319345
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215809757C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214945033C>T , CM000664.2:g.214945033C>T GRCh38
NC_000002.11:g.215809757C>T , CM000664.1:g.215809757C>T GRCh37
NC_000002.10:g.215518002C>T NCBI36
NG_007074.1:g.198395G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.7311G>A (ABCA12) MANE Select ENSP00000272895.7:p.Gln2437=
ENST00000272895.11:c.7311G>A (ABCA12) ENSP00000272895.7:p.Gln2437=
ENST00000389661.4:c.6357G>A (ABCA12) ENSP00000374312.4:p.Gln2119=
NM_015657.3:c.6357G>A (ABCA12) NP_056472.2:p.Gln2119=
NM_173076.2:c.7311G>A (ABCA12) NP_775099.2:p.Gln2437=
NR_103740.1:n.7611G>A (ABCA12)
NR_110292.1:n.322-2792C>T (SNHG31)
XM_011510951.1:c.7320G>A (ABCA12) XP_011509253.1:p.Gln2440=
XM_011510951.2:c.7320G>A (ABCA12) XP_011509253.1:p.Gln2440=
NM_173076.3:c.7311G>A (ABCA12) MANE Select NP_775099.2:p.Gln2437=
NR_103740.2:n.7809G>A (ABCA12)
NM_015657.4:c.6357G>A (ABCA12) NP_056472.2:p.Gln2119=