Canonical Allele Identifier: CA2003794120
Gene: HMBS HGNC NCBI

Linked Data

dbSNP Id: rs1946339834

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119093577A>G , CM000673.2:g.119093577A>G GRCh38
NC_000011.9:g.118964287A>G , CM000673.1:g.118964287A>G GRCh37
NC_000011.8:g.118469497A>G NCBI36
NG_008093.1:g.13701A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.*294A>G ENSP00000509288.1:n.*294A>G