Canonical Allele Identifier: CA2612149496
Gene: HBD HGNC NCBI

Linked Data

gnomAD v4: 11-5234575-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234575A>C , CM000673.2:g.5234575A>C GRCh38
NC_000011.9:g.5255805A>C , CM000673.1:g.5255805A>C GRCh37
NC_000011.8:g.5212381A>C NCBI36
NG_000007.3:g.63041T>G
NG_063112.2:g.14083T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000643122.1:c.-28-114T>G ENSP00000494708.1:n.-28-114T>G
ENST00000380299.3:c.-142T>G ENSP00000369654.3:n.-142T>G
ENST00000429817.1:c.-97-45T>G ENSP00000393810.1:n.-97-45T>G
NM_000519.3:c.-142T>G NP_000510.1:n.-142T>G