Canonical Allele Identifier: CA1949564830
Gene: HBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5233985A= , CM000673.2:g.5233985A= GRCh38
NC_000011.9:g.5255215A= , CM000673.1:g.5255215A= GRCh37
NC_000011.8:g.5211791A= NCBI36
NG_000007.3:g.63631T=
NG_063112.2:g.14673T=

Transcript Alleles

HGVS Amino-acid change
ENST00000643122.1:c.315+6T= ENSP00000494708.1:n.315+6T=
ENST00000650601.1:c.315+6T= MANE Select ENSP00000497529.1:n.315+6T=
ENST00000292901.7:c.315+6T= ENSP00000292901.3:n.315+6T=
ENST00000380299.3:c.315+6T= ENSP00000369654.3:n.315+6T=
ENST00000417377.1:c.92+357T= ENSP00000414741.1:n.92+357T=
NM_000519.3:c.315+6T= NP_000510.1:n.315+6T=
NM_000519.4:c.315+6T= MANE Select NP_000510.1:n.315+6T=