Canonical Allele Identifier: CA431146601
Gene: ABCA12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215928842G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064119G>C , CM000664.2:g.215064119G>C GRCh38
NC_000002.11:g.215928842G>C , CM000664.1:g.215928842G>C GRCh37
NC_000002.10:g.215637087G>C NCBI36
NG_007074.1:g.79310C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.264C>G MANE Select ENSP00000272895.7:p.Gly88=
ENST00000272895.11:c.264C>G ENSP00000272895.7:p.Gly88=
NM_173076.2:c.264C>G NP_775099.2:p.Gly88=
NR_103740.1:n.484C>G
XM_011510951.1:c.264C>G XP_011509253.1:p.Gly88=
XM_011510952.1:c.264C>G XP_011509254.1:p.Gly88=
XM_011510951.2:c.264C>G XP_011509253.1:p.Gly88=
NM_173076.3:c.264C>G MANE Select NP_775099.2:p.Gly88=
NR_103740.2:n.682C>G