Canonical Allele Identifier: CA2612149494

Gene: HBD

Linked Data

• gnomAD v4: 11-5234573-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5234573T>C , CM000673.2:g.5234573T>C	GRCh38
NC_000011.9:g.5255803T>C , CM000673.1:g.5255803T>C	GRCh37
NC_000011.8:g.5212379T>C	NCBI36
NG_000007.3:g.63043A>G
NG_063112.2:g.14085A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000643122.1:c.-28-112A>G	ENSP00000494708.1:n.-28-112A>G
ENST00000380299.3:c.-140A>G	ENSP00000369654.3:n.-140A>G
ENST00000429817.1:c.-97-43A>G	ENSP00000393810.1:n.-97-43A>G
NM_000519.3:c.-140A>G	NP_000510.1:n.-140A>G