Canonical Allele Identifier: CA2003780442
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119084867A= , CM000673.2:g.119084867A= GRCh38
NC_000011.9:g.118955577A= , CM000673.1:g.118955577A= GRCh37
NC_000011.8:g.118460787A= NCBI36
NG_008093.1:g.4991A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536185.5:n.2A=
XM_024448460.1:c.-167A= XP_024304228.1:n.-167A=