Canonical Allele Identifier: CA217113339
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 1097379
ClinVar RCV Id: RCV001418978
dbSNP Id: rs1029676980
gnomAD v3: 11-5226492-C-T
gnomAD v4: 11-5226492-C-T
MyVariant Identifiers: chr11:g.5247722C>T (hg19) chr11:g.5226492C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226492C>T , CM000673.2:g.5226492C>T GRCh38
NC_000011.9:g.5247722C>T , CM000673.1:g.5247722C>T GRCh37
NC_000011.8:g.5204298C>T NCBI36
NG_000007.3:g.71124G>A
NG_059281.1:g.5580G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.315+85G>A ENSP00000494175.1:n.315+85G>A
ENST00000335295.4:c.315+85G>A MANE Select ENSP00000333994.3:n.315+85G>A
ENST00000475226.1:n.247+85G>A
ENST00000485743.1:n.451G>A
ENST00000633227.1:c.*131+85G>A ENSP00000488004.1:n.*131+85G>A
NM_000518.4:c.315+85G>A NP_000509.1:n.315+85G>A
NM_000518.5:c.315+85G>A MANE Select NP_000509.1:n.315+85G>A
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