Canonical Allele Identifier: CA379263486

Gene: HBG2

Linked Data

• MyVariant Identifiers: chr11:g.5274523G>A (hg19) ; chr11:g.5253293G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5253293G>A , CM000673.2:g.5253293G>A	GRCh38
NC_000011.9:g.5274523G>A , CM000673.1:g.5274523G>A	GRCh37
NC_000011.8:g.5231099G>A	NCBI36
NG_000007.3:g.44323C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336906.6:c.428C>T MANE Select	ENSP00000338082.4:p.Ser143Phe
ENST00000380252.6:c.263C>T	ENSP00000369602.2:p.Ser88Phe
ENST00000642908.1:c.315+999C>T	ENSP00000495346.1:n.315+999C>T
ENST00000647543.1:c.378+50C>T	ENSP00000496470.1:n.378+50C>T
ENST00000336906.4:c.428C>T	ENSP00000338082.4:p.Ser143Phe
ENST00000380252.5:c.398C>T	ENSP00000369602.1:p.Ser133Phe
ENST00000380259.6:c.428C>T	ENSP00000369609.2:p.Ser143Phe
ENST00000620888.4:c.315+999C>T	ENSP00000479637.1:n.315+999C>T
NM_000184.2:c.428C>T	NP_000175.1:p.Ser143Phe
NM_000184.3:c.428C>T MANE Select	NP_000175.1:p.Ser143Phe