Canonical Allele Identifier: CA2565293729
Gene: HBG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5254196A>T , CM000673.2:g.5254196A>T GRCh38
NC_000011.9:g.5275426A>T , CM000673.1:g.5275426A>T GRCh37
NC_000011.8:g.5232002A>T NCBI36
NG_000007.3:g.43420T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000336906.6:c.315+96T>A MANE Select ENSP00000338082.4:n.315+96T>A
ENST00000380252.6:c.150+96T>A ENSP00000369602.2:n.150+96T>A
ENST00000642908.1:c.315+96T>A ENSP00000495346.1:n.315+96T>A
ENST00000647543.1:c.315+96T>A ENSP00000496470.1:n.315+96T>A
ENST00000336906.4:c.315+96T>A ENSP00000338082.4:n.315+96T>A
ENST00000380252.5:c.285+96T>A ENSP00000369602.1:n.285+96T>A
ENST00000380259.6:c.315+96T>A ENSP00000369609.2:n.315+96T>A
ENST00000444587.1:c.*184+96T>A ENSP00000488218.1:n.*184+96T>A
ENST00000620888.4:c.315+96T>A ENSP00000479637.1:n.315+96T>A
ENST00000624109.1:c.43-99A>T ENSP00000485458.1:n.43-99A>T
NM_000184.2:c.315+96T>A NP_000175.1:n.315+96T>A
NM_000184.3:c.315+96T>A MANE Select NP_000175.1:n.315+96T>A
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