Canonical Allele Identifier: CA677551598
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 878836
ClinVar RCV Id: RCV001105802 RCV001105803 RCV001105804 RCV001105805
dbSNP Id: rs1345009528
gnomAD v4: 11-5225539-T-C
MyVariant Identifiers: chr11:g.5246769T>C (hg19) chr11:g.5225539T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225539T>C , CM000673.2:g.5225539T>C GRCh38
NC_000011.9:g.5246769T>C , CM000673.1:g.5246769T>C GRCh37
NC_000011.8:g.5203345T>C NCBI36
NG_000007.3:g.72077A>G
NG_059281.1:g.6533A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*59A>G ENSP00000494175.1:n.*59A>G
ENST00000335295.4:c.*59A>G MANE Select ENSP00000333994.3:n.*59A>G
ENST00000633227.1:c.*319A>G ENSP00000488004.1:n.*319A>G
NM_000518.4:c.*59A>G NP_000509.1:n.*59A>G
NM_000518.5:c.*59A>G MANE Select NP_000509.1:n.*59A>G
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