Canonical Allele Identifier: CA1949566322
Gene: HBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234697G= , CM000673.2:g.5234697G= GRCh38
NC_000011.9:g.5255927G= , CM000673.1:g.5255927G= GRCh37
NC_000011.8:g.5212503G= NCBI36
NG_000007.3:g.62919C=
NG_063112.2:g.13961C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000643122.1:c.-28-236C= ENSP00000494708.1:n.-28-236C=
ENST00000429817.1:c.-97-167C= ENSP00000393810.1:n.-97-167C=