Canonical Allele Identifier: CA2832592687
Gene: HBD HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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