Canonical Allele Identifier: CA350458817
Gene: ABCA12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064207G>C , CM000664.2:g.215064207G>C GRCh38
NC_000002.11:g.215928930G>C , CM000664.1:g.215928930G>C GRCh37
NC_000002.10:g.215637175G>C NCBI36
NG_007074.1:g.79222C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.176C>G MANE Select ENSP00000272895.7:p.Pro59Arg
ENST00000272895.11:c.176C>G ENSP00000272895.7:p.Pro59Arg
NM_173076.2:c.176C>G NP_775099.2:p.Pro59Arg
NR_103740.1:n.396C>G
XM_011510951.1:c.176C>G XP_011509253.1:p.Pro59Arg
XM_011510952.1:c.176C>G XP_011509254.1:p.Pro59Arg
XM_011510951.2:c.176C>G XP_011509253.1:p.Pro59Arg
NM_173076.3:c.176C>G MANE Select NP_775099.2:p.Pro59Arg
NR_103740.2:n.594C>G