Canonical Allele Identifier: CA217123856
Gene: HBD HGNC NCBI

Linked Data

dbSNP Id: rs281864561

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234059T>A , CM000673.2:g.5234059T>A GRCh38
NC_000011.9:g.5255289T>A , CM000673.1:g.5255289T>A GRCh37
NC_000011.8:g.5211865T>A NCBI36
NG_000007.3:g.63557A>T
NG_063112.2:g.14599A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643122.1:c.247A>T ENSP00000494708.1:p.Lys83Ter
ENST00000650601.1:c.247A>T MANE Select ENSP00000497529.1:p.Lys83Ter
ENST00000292901.7:c.247A>T ENSP00000292901.3:p.Lys83Ter
ENST00000380299.3:c.247A>T ENSP00000369654.3:p.Lys83Ter
ENST00000417377.1:c.92+283A>T ENSP00000414741.1:n.92+283A>T
ENST00000429817.1:c.247A>T ENSP00000393810.1:p.Lys83Ter
NM_000519.3:c.247A>T NP_000510.1:p.Lys83Ter
NM_000519.4:c.247A>T MANE Select NP_000510.1:p.Lys83Ter