Canonical Allele Identifier: CA124661
Gene: HBD HGNC NCBI

Linked Data

ClinVar Variation Id: 15056
ClinVar RCV Id: RCV000016203
dbSNP Id: rs34460332
gnomAD v4: 11-5234360-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234360C>T , CM000673.2:g.5234360C>T GRCh38
NC_000011.9:g.5255590C>T , CM000673.1:g.5255590C>T GRCh37
NC_000011.8:g.5212166C>T NCBI36
NG_000007.3:g.63256G>A
NG_063112.2:g.14298G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000643122.1:c.74G>A ENSP00000494708.1:p.Gly25Asp
ENST00000650601.1:c.74G>A MANE Select ENSP00000497529.1:p.Gly25Asp
ENST00000292901.7:c.74G>A ENSP00000292901.3:p.Gly25Asp
ENST00000380299.3:c.74G>A ENSP00000369654.3:p.Gly25Asp
ENST00000417377.1:c.74G>A ENSP00000414741.1:p.Gly25Asp
ENST00000429817.1:c.74G>A ENSP00000393810.1:p.Gly25Asp
NM_000519.3:c.74G>A NP_000510.1:p.Gly25Asp
NM_000519.4:c.74G>A MANE Select NP_000510.1:p.Gly25Asp