Canonical Allele Identifier: CA1949587835
Gene: HBG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5253189G= , CM000673.2:g.5253189G= GRCh38
NC_000011.9:g.5274419G= , CM000673.1:g.5274419G= GRCh37
NC_000011.8:g.5230995G= NCBI36
NG_000007.3:g.44427C=

Transcript Alleles

HGVS Amino-acid change
ENST00000336906.6:c.*88C= MANE Select ENSP00000338082.4:n.*88C=
ENST00000642908.1:c.315+1103C= ENSP00000495346.1:n.315+1103C=
ENST00000647543.1:c.378+154C= ENSP00000496470.1:n.378+154C=
ENST00000620888.4:c.315+1103C= ENSP00000479637.1:n.315+1103C=
NM_000184.3:c.*88C= MANE Select NP_000175.1:n.*88C=
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