Canonical Allele Identifier: CA1949566154
Gene: HBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234579T= , CM000673.2:g.5234579T= GRCh38
NC_000011.9:g.5255809T= , CM000673.1:g.5255809T= GRCh37
NC_000011.8:g.5212385T= NCBI36
NG_000007.3:g.63037A=
NG_063112.2:g.14079A=

Transcript Alleles

HGVS Amino-acid change
ENST00000643122.1:c.-28-118A= ENSP00000494708.1:n.-28-118A=
ENST00000380299.3:c.-146A= ENSP00000369654.3:n.-146A=
ENST00000429817.1:c.-97-49A= ENSP00000393810.1:n.-97-49A=
NM_000519.3:c.-146A= NP_000510.1:n.-146A=