Canonical Allele Identifier: CA350458829
Gene: ABCA12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064208G>T , CM000664.2:g.215064208G>T GRCh38
NC_000002.11:g.215928931G>T , CM000664.1:g.215928931G>T GRCh37
NC_000002.10:g.215637176G>T NCBI36
NG_007074.1:g.79221C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.175C>A MANE Select ENSP00000272895.7:p.Pro59Thr
ENST00000272895.11:c.175C>A ENSP00000272895.7:p.Pro59Thr
NM_173076.2:c.175C>A NP_775099.2:p.Pro59Thr
NR_103740.1:n.395C>A
XM_011510951.1:c.175C>A XP_011509253.1:p.Pro59Thr
XM_011510952.1:c.175C>A XP_011509254.1:p.Pro59Thr
XM_011510951.2:c.175C>A XP_011509253.1:p.Pro59Thr
NM_173076.3:c.175C>A MANE Select NP_775099.2:p.Pro59Thr
NR_103740.2:n.593C>A