Canonical Allele Identifier: CA217115065
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 869243
ClinVar RCV Id: RCV001078278
dbSNP Id: rs35684407

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226931T>C , CM000673.2:g.5226931T>C GRCh38
NC_000011.9:g.5248161T>C , CM000673.1:g.5248161T>C GRCh37
NC_000011.8:g.5204737T>C NCBI36
NG_000007.3:g.70685A>G
NG_059281.1:g.5141A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.91A>G ENSP00000494175.1:p.Arg31Gly
ENST00000335295.4:c.91A>G MANE Select ENSP00000333994.3:p.Arg31Gly
ENST00000380315.2:c.91A>G ENSP00000369671.2:p.Arg31Gly
ENST00000485743.1:n.142A>G
ENST00000633227.1:c.76+15A>G ENSP00000488004.1:n.76+15A>G
NM_000518.4:c.91A>G NP_000509.1:p.Arg31Gly
NM_000518.5:c.91A>G MANE Select NP_000509.1:p.Arg31Gly