Canonical Allele Identifier: CA1949566278
Gene: HBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234678C= , CM000673.2:g.5234678C= GRCh38
NC_000011.9:g.5255908C= , CM000673.1:g.5255908C= GRCh37
NC_000011.8:g.5212484C= NCBI36
NG_000007.3:g.62938G=
NG_063112.2:g.13980G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000643122.1:c.-28-217G= ENSP00000494708.1:n.-28-217G=
ENST00000429817.1:c.-97-148G= ENSP00000393810.1:n.-97-148G=