Canonical Allele Identifier: CA1949566257
Gene: HBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234663A= , CM000673.2:g.5234663A= GRCh38
NC_000011.9:g.5255893A= , CM000673.1:g.5255893A= GRCh37
NC_000011.8:g.5212469A= NCBI36
NG_000007.3:g.62953T=
NG_063112.2:g.13995T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000643122.1:c.-28-202T= ENSP00000494708.1:n.-28-202T=
ENST00000429817.1:c.-97-133T= ENSP00000393810.1:n.-97-133T=