Canonical Allele Identifier: CA2612149507
Gene: HBD HGNC NCBI

Linked Data

gnomAD v4: 11-5234585-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234585A>T , CM000673.2:g.5234585A>T GRCh38
NC_000011.9:g.5255815A>T , CM000673.1:g.5255815A>T GRCh37
NC_000011.8:g.5212391A>T NCBI36
NG_000007.3:g.63031T>A
NG_063112.2:g.14073T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000643122.1:c.-28-124T>A ENSP00000494708.1:n.-28-124T>A
ENST00000380299.3:c.-152T>A ENSP00000369654.3:n.-152T>A
ENST00000429817.1:c.-97-55T>A ENSP00000393810.1:n.-97-55T>A
NM_000519.3:c.-152T>A NP_000510.1:n.-152T>A