Canonical Allele Identifier: CA1949566078
Community Standard Title: NC_000011.10:g.5234514T=
Gene: HBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234514T= , CM000673.2:g.5234514T= GRCh38
NC_000011.9:g.5255744T= , CM000673.1:g.5255744T= GRCh37
NC_000011.8:g.5212320T= NCBI36
NG_000007.3:g.63102A=
NG_063112.2:g.14144A=

Transcript Alleles

HGVS Amino-acid Change
NM_000519.3:c.-81A= NP_000510.1:n.-81A=
ENST00000380299.3:c.-81A= ENSP00000369654.3:n.-81A=
ENST00000429817.1:c.-81A= ENSP00000393810.1:n.-81A=
ENST00000643122.1:c.-28-53A= ENSP00000494708.1:n.-28-53A=