Canonical Allele Identifier: CA677537145
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs367723569
gnomAD v3: 11-5226927-A-T
gnomAD v4: 11-5226927-A-T
MyVariant Identifiers: chr11:g.5248157A>T (hg19) chr11:g.5226927A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226927A>T , CM000673.2:g.5226927A>T GRCh38
NC_000011.9:g.5248157A>T , CM000673.1:g.5248157A>T GRCh37
NC_000011.8:g.5204733A>T NCBI36
NG_000007.3:g.70689T>A
NG_059281.1:g.5145T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.92+3T>A ENSP00000494175.1:n.92+3T>A
ENST00000335295.4:c.92+3T>A MANE Select ENSP00000333994.3:n.92+3T>A
ENST00000380315.2:c.92+3T>A ENSP00000369671.2:n.92+3T>A
ENST00000485743.1:n.143+3T>A
ENST00000633227.1:c.76+19T>A ENSP00000488004.1:n.76+19T>A
NM_000518.4:c.92+3T>A NP_000509.1:n.92+3T>A
NM_000518.5:c.92+3T>A MANE Select NP_000509.1:n.92+3T>A
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