Canonical Allele Identifier: CA2612149510
Gene: HBD HGNC NCBI

Linked Data

gnomAD v4: 11-5234587-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234587T>A , CM000673.2:g.5234587T>A GRCh38
NC_000011.9:g.5255817T>A , CM000673.1:g.5255817T>A GRCh37
NC_000011.8:g.5212393T>A NCBI36
NG_000007.3:g.63029A>T
NG_063112.2:g.14071A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000643122.1:c.-28-126A>T ENSP00000494708.1:n.-28-126A>T
ENST00000380299.3:c.-154A>T ENSP00000369654.3:n.-154A>T
ENST00000429817.1:c.-97-57A>T ENSP00000393810.1:n.-97-57A>T
NM_000519.3:c.-154A>T NP_000510.1:n.-154A>T