Canonical Allele Identifier: CA1949566142
Gene: HBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234571C= , CM000673.2:g.5234571C= GRCh38
NC_000011.9:g.5255801C= , CM000673.1:g.5255801C= GRCh37
NC_000011.8:g.5212377C= NCBI36
NG_000007.3:g.63045G=
NG_063112.2:g.14087G=

Transcript Alleles

HGVS Amino-acid change
ENST00000643122.1:c.-28-110G= ENSP00000494708.1:n.-28-110G=
ENST00000380299.3:c.-138G= ENSP00000369654.3:n.-138G=
ENST00000429817.1:c.-97-41G= ENSP00000393810.1:n.-97-41G=
NM_000519.3:c.-138G= NP_000510.1:n.-138G=