Canonical Allele Identifier: CA2616356102
Gene: HMBS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119093639G>T , CM000673.2:g.119093639G>T GRCh38
NC_000011.9:g.118964349G>T , CM000673.1:g.118964349G>T GRCh37
NC_000011.8:g.118469559G>T NCBI36
NG_008093.1:g.13763G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.*356G>T ENSP00000509288.1:n.*356G>T