Canonical Allele Identifier: CA124908
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15199
ClinVar RCV Id: RCV000016382
dbSNP Id: rs33991059

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226779C>G , CM000673.2:g.5226779C>G GRCh38
NC_000011.9:g.5248009C>G , CM000673.1:g.5248009C>G GRCh37
NC_000011.8:g.5204585C>G NCBI36
NG_000007.3:g.70837G>C
NG_059281.1:g.5293G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.113G>C ENSP00000494175.1:p.Trp38Ser
ENST00000335295.4:c.113G>C MANE Select ENSP00000333994.3:p.Trp38Ser
ENST00000380315.2:c.113G>C ENSP00000369671.2:p.Trp38Ser
ENST00000475226.1:n.45G>C
ENST00000485743.1:n.164G>C
ENST00000633227.1:c.97G>C ENSP00000488004.1:p.Gly33Arg
NM_000518.4:c.113G>C NP_000509.1:p.Trp38Ser
NM_000518.5:c.113G>C MANE Select NP_000509.1:p.Trp38Ser