Canonical Allele Identifier: CA431148685
Gene: ABCA12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215845246G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214980522G>T , CM000664.2:g.214980522G>T GRCh38
NC_000002.11:g.215845246G>T , CM000664.1:g.215845246G>T GRCh37
NC_000002.10:g.215553491G>T NCBI36
NG_007074.1:g.162906C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.4701C>A MANE Select ENSP00000272895.7:p.Ala1567=
ENST00000272895.11:c.4701C>A ENSP00000272895.7:p.Ala1567=
ENST00000389661.4:c.3747C>A ENSP00000374312.4:p.Ala1249=
NM_015657.3:c.3747C>A NP_056472.2:p.Ala1249=
NM_173076.2:c.4701C>A NP_775099.2:p.Ala1567=
NR_103740.1:n.5001C>A
XM_011510951.1:c.4710C>A XP_011509253.1:p.Ala1570=
XM_011510952.1:c.4710C>A XP_011509254.1:p.Ala1570=
XM_011510951.2:c.4710C>A XP_011509253.1:p.Ala1570=
NM_173076.3:c.4701C>A MANE Select NP_775099.2:p.Ala1567=
NR_103740.2:n.5199C>A
NM_015657.4:c.3747C>A NP_056472.2:p.Ala1249=