Canonical Allele Identifier: CA2739276168
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 2829919
ClinVar RCV Id: RCV003678572
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226453C>G , CM000673.2:g.5226453C>G GRCh38
NC_000011.9:g.5247683C>G , CM000673.1:g.5247683C>G GRCh37
NC_000011.8:g.5204259C>G NCBI36
NG_000007.3:g.71163G>C
NG_059281.1:g.5619G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.315+124G>C ENSP00000494175.1:n.315+124G>C
ENST00000335295.4:c.315+124G>C MANE Select ENSP00000333994.3:n.315+124G>C
ENST00000475226.1:n.247+124G>C
ENST00000485743.1:n.490G>C
ENST00000633227.1:c.*131+124G>C ENSP00000488004.1:n.*131+124G>C
NM_000518.4:c.315+124G>C NP_000509.1:n.315+124G>C
NM_000518.5:c.315+124G>C MANE Select NP_000509.1:n.315+124G>C
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