Canonical Allele Identifier: CA2844623030
Gene: HBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234518G>C , CM000673.2:g.5234518G>C GRCh38
NC_000011.9:g.5255748G>C , CM000673.1:g.5255748G>C GRCh37
NC_000011.8:g.5212324G>C NCBI36
NG_000007.3:g.63098C>G
NG_063112.2:g.14140C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000643122.1:c.-28-57C>G ENSP00000494708.1:n.-28-57C>G
ENST00000380299.3:c.-85C>G ENSP00000369654.3:n.-85C>G
ENST00000429817.1:c.-85C>G ENSP00000393810.1:n.-85C>G
NM_000519.3:c.-85C>G NP_000510.1:n.-85C>G