Canonical Allele Identifier: CA379276718
Gene: HBD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5233996A>T , CM000673.2:g.5233996A>T GRCh38
NC_000011.9:g.5255226A>T , CM000673.1:g.5255226A>T GRCh37
NC_000011.8:g.5211802A>T NCBI36
NG_000007.3:g.63620T>A
NG_063112.2:g.14662T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000643122.1:c.310T>A ENSP00000494708.1:p.Phe104Ile
ENST00000650601.1:c.310T>A MANE Select ENSP00000497529.1:p.Phe104Ile
ENST00000292901.7:c.310T>A ENSP00000292901.3:p.Phe104Ile
ENST00000380299.3:c.310T>A ENSP00000369654.3:p.Phe104Ile
ENST00000417377.1:c.92+346T>A ENSP00000414741.1:n.92+346T>A
ENST00000429817.1:c.310T>A ENSP00000393810.1:p.Phe104Ile
NM_000519.3:c.310T>A NP_000510.1:p.Phe104Ile
NM_000519.4:c.310T>A MANE Select NP_000510.1:p.Phe104Ile