Canonical Allele Identifier: CA5839927
Gene: HBD HGNC NCBI

Linked Data

dbSNP Id: rs762198004
gnomAD v2: 11-5255222-C-T
gnomAD v3: 11-5233992-C-T
gnomAD v4: 11-5233992-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5233992C>T , CM000673.2:g.5233992C>T GRCh38
NC_000011.9:g.5255222C>T , CM000673.1:g.5255222C>T GRCh37
NC_000011.8:g.5211798C>T NCBI36
NG_000007.3:g.63624G>A
NG_063112.2:g.14666G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000643122.1:c.314G>A ENSP00000494708.1:p.Arg105Lys
ENST00000650601.1:c.314G>A MANE Select ENSP00000497529.1:p.Arg105Lys
ENST00000292901.7:c.314G>A ENSP00000292901.3:p.Arg105Lys
ENST00000380299.3:c.314G>A ENSP00000369654.3:p.Arg105Lys
ENST00000417377.1:c.92+350G>A ENSP00000414741.1:n.92+350G>A
NM_000519.3:c.314G>A NP_000510.1:p.Arg105Lys
NM_000519.4:c.314G>A MANE Select NP_000510.1:p.Arg105Lys