Canonical Allele Identifier: CA2003794238
Gene: HMBS HGNC NCBI

Linked Data

dbSNP Id: rs1946342169
gnomAD v4: 11-119093645-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119093645C>T , CM000673.2:g.119093645C>T GRCh38
NC_000011.9:g.118964355C>T , CM000673.1:g.118964355C>T GRCh37
NC_000011.8:g.118469565C>T NCBI36
NG_008093.1:g.13769C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.*362C>T ENSP00000509288.1:n.*362C>T
Search 100 bp 5'
Search 100 bp 3'