Canonical Allele Identifier: CA677767932
Gene: HBG2 HGNC NCBI

Linked Data

dbSNP Id: rs1272082344
MyVariant Identifiers: chr11:g.5271311A>T (hg19) chr11:g.5250081A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5250081A>T , CM000673.2:g.5250081A>T GRCh38
NC_000011.9:g.5271311A>T , CM000673.1:g.5271311A>T GRCh37
NC_000011.8:g.5227887A>T NCBI36
NG_000007.3:g.47535T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1594T>A ENSP00000495346.1:n.316-1594T>A
ENST00000647543.1:c.379-1594T>A ENSP00000496470.1:n.379-1594T>A
ENST00000620888.4:c.316-1594T>A ENSP00000479637.1:n.316-1594T>A
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