Canonical Allele Identifier: CA10587128
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 256347
ClinVar RCV Id: RCV000248556 RCV000625739 RCV000864684
dbSNP Id: rs558554234
gnomAD v2: 11-5247194-G-A
gnomAD v3: 11-5225964-G-A
gnomAD v4: 11-5225964-G-A
MyVariant Identifiers: chr11:g.5247194G>A (hg19) chr11:g.5225964G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225964G>A , CM000673.2:g.5225964G>A GRCh38
NC_000011.9:g.5247194G>A , CM000673.1:g.5247194G>A GRCh37
NC_000011.8:g.5203770G>A NCBI36
NG_000007.3:g.71652C>T
NG_059281.1:g.6108C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.316-238C>T ENSP00000494175.1:n.316-238C>T
ENST00000335295.4:c.316-238C>T MANE Select ENSP00000333994.3:n.316-238C>T
ENST00000475226.1:n.248-238C>T
ENST00000633227.1:c.*132-238C>T ENSP00000488004.1:n.*132-238C>T
NM_000518.4:c.316-238C>T NP_000509.1:n.316-238C>T
NM_000518.5:c.316-238C>T MANE Select NP_000509.1:n.316-238C>T
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