Canonical Allele Identifier: CA677552453
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 633253
ClinVar RCV Id: RCV000781434 RCV001481699
dbSNP Id: rs1280140490
gnomAD v3: 11-5225753-A-C
gnomAD v4: 11-5225753-A-C
MyVariant Identifiers: chr11:g.5246983A>C (hg19) chr11:g.5225753A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225753A>C , CM000673.2:g.5225753A>C GRCh38
NC_000011.9:g.5246983A>C , CM000673.1:g.5246983A>C GRCh37
NC_000011.8:g.5203559A>C NCBI36
NG_000007.3:g.71863T>G
NG_059281.1:g.6319T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.316-27T>G ENSP00000494175.1:n.316-27T>G
ENST00000335295.4:c.316-27T>G MANE Select ENSP00000333994.3:n.316-27T>G
ENST00000475226.1:n.248-27T>G
ENST00000633227.1:c.*132-27T>G ENSP00000488004.1:n.*132-27T>G
NM_000518.4:c.316-27T>G NP_000509.1:n.316-27T>G
NM_000518.5:c.316-27T>G MANE Select NP_000509.1:n.316-27T>G
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