Canonical Allele Identifier: CA934688348
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs1589893853
gnomAD v3: 11-5227177-A-G
gnomAD v4: 11-5227177-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227177A>G , CM000673.2:g.5227177A>G GRCh38
NC_000011.9:g.5248407A>G , CM000673.1:g.5248407A>G GRCh37
NC_000011.8:g.5204983A>G NCBI36
NG_000007.3:g.70439T>C
NG_059281.1:g.4895T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-156T>C ENSP00000494175.1:n.-156T>C
ENST00000380315.2:c.-18-138T>C ENSP00000369671.2:n.-18-138T>C