Canonical Allele Identifier: CA379264912

Gene: HBG2

Linked Data

• MyVariant Identifiers: chr11:g.5275866C>A (hg19) ; chr11:g.5254636C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254636C>A , CM000673.2:g.5254636C>A	GRCh38
NC_000011.9:g.5275866C>A , CM000673.1:g.5275866C>A	GRCh37
NC_000011.8:g.5232442C>A	NCBI36
NG_000007.3:g.42980G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.92+1G>T MANE Select	ENSP00000338082.4:n.92+1G>T
ENST00000380252.6:c.-73-122G>T	ENSP00000369602.2:n.-73-122G>T
ENST00000380259.7:c.1638+1G>T	ENSP00000369609.3:n.1638+1G>T
ENST00000642908.1:c.92+1G>T	ENSP00000495346.1:n.92+1G>T
ENST00000647543.1:c.92+1G>T	ENSP00000496470.1:n.92+1G>T
ENST00000336906.4:c.92+1G>T	ENSP00000338082.4:n.92+1G>T
ENST00000380252.5:c.63-122G>T	ENSP00000369602.1:n.63-122G>T
ENST00000380259.6:c.92+1G>T	ENSP00000369609.2:n.92+1G>T
ENST00000444587.1:c.54+39G>T	ENSP00000488218.1:n.54+39G>T
ENST00000620888.4:c.92+1G>T	ENSP00000479637.1:n.92+1G>T
ENST00000624109.1:c.265C>A	ENSP00000485458.1:p.Pro89Thr
NM_000184.2:c.92+1G>T	NP_000175.1:n.92+1G>T
NM_000184.3:c.92+1G>T MANE Select	NP_000175.1:n.92+1G>T