Canonical Allele Identifier: CA2579830079
Gene: HBG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5250059G>T , CM000673.2:g.5250059G>T GRCh38
NC_000011.9:g.5271289G>T , CM000673.1:g.5271289G>T GRCh37
NC_000011.8:g.5227865G>T NCBI36
NG_000007.3:g.47557C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1572C>A ENSP00000495346.1:n.316-1572C>A
ENST00000647543.1:c.379-1572C>A ENSP00000496470.1:n.379-1572C>A
ENST00000620888.4:c.316-1572C>A ENSP00000479637.1:n.316-1572C>A
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