Canonical Allele Identifier: CA2612162006
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 2760286
ClinVar RCV Id: RCV003572095
gnomAD v4: 11-5226355-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226355G>T , CM000673.2:g.5226355G>T GRCh38
NC_000011.9:g.5247585G>T , CM000673.1:g.5247585G>T GRCh37
NC_000011.8:g.5204161G>T NCBI36
NG_000007.3:g.71261C>A
NG_059281.1:g.5717C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.315+222C>A ENSP00000494175.1:n.315+222C>A
ENST00000335295.4:c.315+222C>A MANE Select ENSP00000333994.3:n.315+222C>A
ENST00000475226.1:n.247+222C>A
ENST00000485743.1:n.588C>A
ENST00000633227.1:c.*131+222C>A ENSP00000488004.1:n.*131+222C>A
NM_000518.4:c.315+222C>A NP_000509.1:n.315+222C>A
NM_000518.5:c.315+222C>A MANE Select NP_000509.1:n.315+222C>A
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