Canonical Allele Identifier: CA2574735644
Gene: HBD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5233931del , CM000673.2:g.5233931del GRCh38
NC_000011.9:g.5255161del , CM000673.1:g.5255161del GRCh37
NC_000011.8:g.5211737del NCBI36
NG_000007.3:g.63688del
NG_063112.2:g.14730del

Transcript Alleles

HGVS Amino-acid change
ENST00000643122.1:c.315+63del ENSP00000494708.1:n.315+63del
ENST00000650601.1:c.315+63del MANE Select ENSP00000497529.1:n.315+63del
ENST00000292901.7:c.315+63del ENSP00000292901.3:n.315+63del
ENST00000380299.3:c.315+63del ENSP00000369654.3:n.315+63del
ENST00000417377.1:c.92+414del ENSP00000414741.1:n.92+414del
NM_000519.3:c.315+63del NP_000510.1:n.315+63del
NM_000519.4:c.315+63del MANE Select NP_000510.1:n.315+63del