Canonical Allele Identifier: CA125338
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15482
ClinVar RCV Id: RCV000016740
dbSNP Id: rs35286210
MyVariant Identifiers: chr11:g.5247893C>G (hg19) chr11:g.5226663C>G (hg38)
PubMed: PMID:2268685
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226663C>G , CM000673.2:g.5226663C>G GRCh38
NC_000011.9:g.5247893C>G , CM000673.1:g.5247893C>G GRCh37
NC_000011.8:g.5204469C>G NCBI36
NG_000007.3:g.70953G>C
NG_059281.1:g.5409G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.229G>C ENSP00000494175.1:p.Ala77Pro
ENST00000335295.4:c.229G>C MANE Select ENSP00000333994.3:p.Ala77Pro
ENST00000380315.2:c.229G>C ENSP00000369671.2:p.Ala77Pro
ENST00000475226.1:n.161G>C
ENST00000485743.1:n.280G>C
ENST00000633227.1:c.*45G>C ENSP00000488004.1:n.*45G>C
NM_000518.4:c.229G>C NP_000509.1:p.Ala77Pro
NM_000518.5:c.229G>C MANE Select NP_000509.1:p.Ala77Pro
Search 100 bp 5'
Search 100 bp 3'