Canonical Allele Identifier: CA2612149396
Gene: HBD HGNC NCBI

Linked Data

dbSNP Id: rs2133596808
gnomAD v4: 11-5234482-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234482G>A , CM000673.2:g.5234482G>A GRCh38
NC_000011.9:g.5255712G>A , CM000673.1:g.5255712G>A GRCh37
NC_000011.8:g.5212288G>A NCBI36
NG_000007.3:g.63134C>T
NG_063112.2:g.14176C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000643122.1:c.-28-21C>T ENSP00000494708.1:n.-28-21C>T
ENST00000650601.1:c.-49C>T MANE Select ENSP00000497529.1:n.-49C>T
ENST00000292901.7:c.-49C>T ENSP00000292901.3:n.-49C>T
ENST00000380299.3:c.-49C>T ENSP00000369654.3:n.-49C>T
ENST00000417377.1:c.-49C>T ENSP00000414741.1:n.-49C>T
ENST00000429817.1:c.-49C>T ENSP00000393810.1:n.-49C>T
NM_000519.3:c.-49C>T NP_000510.1:n.-49C>T
NM_000519.4:c.-49C>T MANE Select NP_000510.1:n.-49C>T