Canonical Allele Identifier: CA2612149607
Gene: HBD HGNC NCBI

Linked Data

gnomAD v4: 11-5234667-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234667A>G , CM000673.2:g.5234667A>G GRCh38
NC_000011.9:g.5255897A>G , CM000673.1:g.5255897A>G GRCh37
NC_000011.8:g.5212473A>G NCBI36
NG_000007.3:g.62949T>C
NG_063112.2:g.13991T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000643122.1:c.-28-206T>C ENSP00000494708.1:n.-28-206T>C
ENST00000429817.1:c.-97-137T>C ENSP00000393810.1:n.-97-137T>C