Canonical Allele Identifier: CA350458225
Gene: ABCA12 HGNC NCBI

Linked Data

dbSNP Id: rs1701590549

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064106G>A , CM000664.2:g.215064106G>A GRCh38
NC_000002.11:g.215928829G>A , CM000664.1:g.215928829G>A GRCh37
NC_000002.10:g.215637074G>A NCBI36
NG_007074.1:g.79323C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.277C>T MANE Select ENSP00000272895.7:p.Leu93Phe
ENST00000272895.11:c.277C>T ENSP00000272895.7:p.Leu93Phe
NM_173076.2:c.277C>T NP_775099.2:p.Leu93Phe
NR_103740.1:n.497C>T
XM_011510951.1:c.277C>T XP_011509253.1:p.Leu93Phe
XM_011510952.1:c.277C>T XP_011509254.1:p.Leu93Phe
XM_011510951.2:c.277C>T XP_011509253.1:p.Leu93Phe
NM_173076.3:c.277C>T MANE Select NP_775099.2:p.Leu93Phe
NR_103740.2:n.695C>T