Canonical Allele Identifier: CA125486
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15582
ClinVar RCV Id: RCV000016849
dbSNP Id: rs34049764
MyVariant Identifiers: chr11:g.5246923G>A (hg19) chr11:g.5225693G>A (hg38)
PubMed: PMID:10870882 PMID:11300344
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225693G>A , CM000673.2:g.5225693G>A GRCh38
NC_000011.9:g.5246923G>A , CM000673.1:g.5246923G>A GRCh37
NC_000011.8:g.5203499G>A NCBI36
NG_000007.3:g.71923C>T
NG_059281.1:g.6379C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.349C>T ENSP00000494175.1:p.His117Tyr
ENST00000335295.4:c.349C>T MANE Select ENSP00000333994.3:p.His117Tyr
ENST00000475226.1:n.281C>T
ENST00000633227.1:c.*165C>T ENSP00000488004.1:n.*165C>T
NM_000518.4:c.349C>T NP_000509.1:p.His117Tyr
NM_000518.5:c.349C>T MANE Select NP_000509.1:p.His117Tyr
Search 100 bp 5'
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