Canonical Allele Identifier: CA2838898131
Gene: HBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234522C>A , CM000673.2:g.5234522C>A GRCh38
NC_000011.9:g.5255752C>A , CM000673.1:g.5255752C>A GRCh37
NC_000011.8:g.5212328C>A NCBI36
NG_000007.3:g.63094G>T
NG_063112.2:g.14136G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643122.1:c.-28-61G>T ENSP00000494708.1:n.-28-61G>T
ENST00000380299.3:c.-89G>T ENSP00000369654.3:n.-89G>T
ENST00000429817.1:c.-89G>T ENSP00000393810.1:n.-89G>T
NM_000519.3:c.-89G>T NP_000510.1:n.-89G>T