Canonical Allele Identifier: CA658683677
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 496007
ClinVar RCV Id: RCV000587266
dbSNP Id: rs1377832836
gnomAD v3: 11-5226926-C-T
gnomAD v4: 11-5226926-C-T
MyVariant Identifiers: chr11:g.5248156C>T (hg19) chr11:g.5226926C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226926C>T , CM000673.2:g.5226926C>T GRCh38
NC_000011.9:g.5248156C>T , CM000673.1:g.5248156C>T GRCh37
NC_000011.8:g.5204732C>T NCBI36
NG_000007.3:g.70690G>A
NG_059281.1:g.5146G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.92+4G>A ENSP00000494175.1:n.92+4G>A
ENST00000335295.4:c.92+4G>A MANE Select ENSP00000333994.3:n.92+4G>A
ENST00000380315.2:c.92+4G>A ENSP00000369671.2:n.92+4G>A
ENST00000485743.1:n.143+4G>A
ENST00000633227.1:c.76+20G>A ENSP00000488004.1:n.76+20G>A
NM_000518.4:c.92+4G>A NP_000509.1:n.92+4G>A
NM_000518.5:c.92+4G>A MANE Select NP_000509.1:n.92+4G>A
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