Canonical Allele Identifier: CA2616356032
Gene: HMBS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119093604C>T , CM000673.2:g.119093604C>T GRCh38
NC_000011.9:g.118964314C>T , CM000673.1:g.118964314C>T GRCh37
NC_000011.8:g.118469524C>T NCBI36
NG_008093.1:g.13728C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.*321C>T ENSP00000509288.1:n.*321C>T