Canonical Allele Identifier: CA1949566227
Gene: HBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234648T= , CM000673.2:g.5234648T= GRCh38
NC_000011.9:g.5255878T= , CM000673.1:g.5255878T= GRCh37
NC_000011.8:g.5212454T= NCBI36
NG_000007.3:g.62968A=
NG_063112.2:g.14010A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000643122.1:c.-28-187A= ENSP00000494708.1:n.-28-187A=
ENST00000380299.3:c.-215A= ENSP00000369654.3:n.-215A=
ENST00000429817.1:c.-97-118A= ENSP00000393810.1:n.-97-118A=