Canonical Allele Identifier: CA350458324
Gene: ABCA12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064120C>A , CM000664.2:g.215064120C>A GRCh38
NC_000002.11:g.215928843C>A , CM000664.1:g.215928843C>A GRCh37
NC_000002.10:g.215637088C>A NCBI36
NG_007074.1:g.79309G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.263G>T MANE Select ENSP00000272895.7:p.Gly88Val
ENST00000272895.11:c.263G>T ENSP00000272895.7:p.Gly88Val
NM_173076.2:c.263G>T NP_775099.2:p.Gly88Val
NR_103740.1:n.483G>T
XM_011510951.1:c.263G>T XP_011509253.1:p.Gly88Val
XM_011510952.1:c.263G>T XP_011509254.1:p.Gly88Val
XM_011510951.2:c.263G>T XP_011509253.1:p.Gly88Val
NM_173076.3:c.263G>T MANE Select NP_775099.2:p.Gly88Val
NR_103740.2:n.681G>T