Canonical Allele Identifier: CA379276708
Gene: HBD HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000643122.1:c.314G>C ENSP00000494708.1:p.Arg105Thr
ENST00000650601.1:c.314G>C MANE Select ENSP00000497529.1:p.Arg105Thr
ENST00000292901.7:c.314G>C ENSP00000292901.3:p.Arg105Thr
ENST00000380299.3:c.314G>C ENSP00000369654.3:p.Arg105Thr
ENST00000417377.1:c.92+350G>C ENSP00000414741.1:n.92+350G>C
NM_000519.3:c.314G>C NP_000510.1:p.Arg105Thr
NM_000519.4:c.314G>C MANE Select NP_000510.1:p.Arg105Thr