Canonical Allele Identifier: CA350458844
Gene: ABCA12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215064213A>C , CM000664.2:g.215064213A>C GRCh38
NC_000002.11:g.215928936A>C , CM000664.1:g.215928936A>C GRCh37
NC_000002.10:g.215637181A>C NCBI36
NG_007074.1:g.79216T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272895.12:c.170T>G MANE Select ENSP00000272895.7:p.Leu57Arg
ENST00000272895.11:c.170T>G ENSP00000272895.7:p.Leu57Arg
NM_173076.2:c.170T>G NP_775099.2:p.Leu57Arg
NR_103740.1:n.390T>G
XM_011510951.1:c.170T>G XP_011509253.1:p.Leu57Arg
XM_011510952.1:c.170T>G XP_011509254.1:p.Leu57Arg
XM_011510951.2:c.170T>G XP_011509253.1:p.Leu57Arg
NM_173076.3:c.170T>G MANE Select NP_775099.2:p.Leu57Arg
NR_103740.2:n.588T>G