Canonical Allele Identifier: CA13414124
Gene: CAT HGNC NCBI

Linked Data

dbSNP Id: rs7943316

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34438925A>T , CM000673.2:g.34438925A>T GRCh38
NC_000011.9:g.34460472A>T , CM000673.1:g.34460472A>T GRCh37
NC_000011.8:g.34417048A>T NCBI36
NG_013339.1:g.5001A>T
NG_013339.2:g.5001A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000241052.4:c.-89A>T ENSP00000241052.4:n.-89A>T
NM_001752.3:c.-89A>T NP_001743.1:n.-89A>T