Canonical Allele Identifier: CA217113100
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 1119111
ClinVar RCV Id: RCV001448478
dbSNP Id: rs892640661
gnomAD v3: 11-5226181-T-C
gnomAD v4: 11-5226181-T-C
MyVariant Identifiers: chr11:g.5247411T>C (hg19) chr11:g.5226181T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226181T>C , CM000673.2:g.5226181T>C GRCh38
NC_000011.9:g.5247411T>C , CM000673.1:g.5247411T>C GRCh37
NC_000011.8:g.5203987T>C NCBI36
NG_000007.3:g.71435A>G
NG_059281.1:g.5891A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.315+396A>G ENSP00000494175.1:n.315+396A>G
ENST00000335295.4:c.315+396A>G MANE Select ENSP00000333994.3:n.315+396A>G
ENST00000475226.1:n.247+396A>G
ENST00000633227.1:c.*131+396A>G ENSP00000488004.1:n.*131+396A>G
NM_000518.4:c.315+396A>G NP_000509.1:n.315+396A>G
NM_000518.5:c.315+396A>G MANE Select NP_000509.1:n.315+396A>G
Search 100 bp 5'
Search 100 bp 3'