Canonical Allele Identifier: CA2612149485
Gene: HBD HGNC NCBI

Linked Data

gnomAD v4: 11-5234565-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234565G>A , CM000673.2:g.5234565G>A GRCh38
NC_000011.9:g.5255795G>A , CM000673.1:g.5255795G>A GRCh37
NC_000011.8:g.5212371G>A NCBI36
NG_000007.3:g.63051C>T
NG_063112.2:g.14093C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000643122.1:c.-28-104C>T ENSP00000494708.1:n.-28-104C>T
ENST00000380299.3:c.-132C>T ENSP00000369654.3:n.-132C>T
ENST00000429817.1:c.-97-35C>T ENSP00000393810.1:n.-97-35C>T
NM_000519.3:c.-132C>T NP_000510.1:n.-132C>T