Canonical Allele Identifier: CA124708
Gene: HBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234559T>A , CM000673.2:g.5234559T>A GRCh38
NC_000011.9:g.5255789T>A , CM000673.1:g.5255789T>A GRCh37
NC_000011.8:g.5212365T>A NCBI36
NG_000007.3:g.63057A>T
NG_063112.2:g.14099A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643122.1:c.-28-98A>T ENSP00000494708.1:n.-28-98A>T
ENST00000380299.3:c.-126A>T ENSP00000369654.3:n.-126A>T
ENST00000429817.1:c.-97-29A>T ENSP00000393810.1:n.-97-29A>T
NM_000519.3:c.-126A>T NP_000510.1:n.-126A>T