Canonical Allele Identifier: CA350458860
Gene: ABCA12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064217A>T , CM000664.2:g.215064217A>T GRCh38
NC_000002.11:g.215928940A>T , CM000664.1:g.215928940A>T GRCh37
NC_000002.10:g.215637185A>T NCBI36
NG_007074.1:g.79212T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.166T>A MANE Select ENSP00000272895.7:p.Tyr56Asn
ENST00000272895.11:c.166T>A ENSP00000272895.7:p.Tyr56Asn
NM_173076.2:c.166T>A NP_775099.2:p.Tyr56Asn
NR_103740.1:n.386T>A
XM_011510951.1:c.166T>A XP_011509253.1:p.Tyr56Asn
XM_011510952.1:c.166T>A XP_011509254.1:p.Tyr56Asn
XM_011510951.2:c.166T>A XP_011509253.1:p.Tyr56Asn
NM_173076.3:c.166T>A MANE Select NP_775099.2:p.Tyr56Asn
NR_103740.2:n.584T>A