Canonical Allele Identifier: CA379264769

Gene: HBG2

Linked Data

• MyVariant Identifiers: chr11:g.5275734C>G (hg19) ; chr11:g.5254504C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254504C>G , CM000673.2:g.5254504C>G	GRCh38
NC_000011.9:g.5275734C>G , CM000673.1:g.5275734C>G	GRCh37
NC_000011.8:g.5232310C>G	NCBI36
NG_000007.3:g.43112G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336906.6:c.103G>C MANE Select	ENSP00000338082.4:p.Val35Leu
ENST00000380252.6:c.-63G>C	ENSP00000369602.2:n.-63G>C
ENST00000380259.7:c.1649G>C	ENSP00000369609.3:n.1649G>C
ENST00000642908.1:c.103G>C	ENSP00000495346.1:p.Val35Leu
ENST00000647543.1:c.103G>C	ENSP00000496470.1:p.Val35Leu
ENST00000336906.4:c.103G>C	ENSP00000338082.4:p.Val35Leu
ENST00000380252.5:c.73G>C	ENSP00000369602.1:p.Val25Leu
ENST00000380259.6:c.103G>C	ENSP00000369609.2:p.Val35Leu
ENST00000444587.1:c.65G>C	ENSP00000488218.1:p.Cys22Ser
ENST00000620888.4:c.103G>C	ENSP00000479637.1:p.Val35Leu
ENST00000624109.1:c.252C>G	ENSP00000485458.1:p.Asp84Glu
NM_000184.2:c.103G>C	NP_000175.1:p.Val35Leu
NM_000184.3:c.103G>C MANE Select	NP_000175.1:p.Val35Leu