Canonical Allele Identifier: CA677772184

Gene: HBG2

Linked Data

• dbSNP Id: rs1201210171
• gnomAD v4: 11-5254547-G-C
• MyVariant Identifiers: chr11:g.5275777G>C (hg19) ; chr11:g.5254547G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254547G>C , CM000673.2:g.5254547G>C	GRCh38
NC_000011.9:g.5275777G>C , CM000673.1:g.5275777G>C	GRCh37
NC_000011.8:g.5232353G>C	NCBI36
NG_000007.3:g.43069C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.93-33C>G MANE Select	ENSP00000338082.4:n.93-33C>G
ENST00000380252.6:c.-73-33C>G	ENSP00000369602.2:n.-73-33C>G
ENST00000380259.7:c.1639-33C>G	ENSP00000369609.3:n.1639-33C>G
ENST00000642908.1:c.93-33C>G	ENSP00000495346.1:n.93-33C>G
ENST00000647543.1:c.93-33C>G	ENSP00000496470.1:n.93-33C>G
ENST00000336906.4:c.93-33C>G	ENSP00000338082.4:n.93-33C>G
ENST00000380252.5:c.63-33C>G	ENSP00000369602.1:n.63-33C>G
ENST00000380259.6:c.93-33C>G	ENSP00000369609.2:n.93-33C>G
ENST00000444587.1:c.55-33C>G	ENSP00000488218.1:n.55-33C>G
ENST00000620888.4:c.93-33C>G	ENSP00000479637.1:n.93-33C>G
ENST00000624109.1:c.264+31G>C	ENSP00000485458.1:n.264+31G>C
NM_000184.2:c.93-33C>G	NP_000175.1:n.93-33C>G
NM_000184.3:c.93-33C>G MANE Select	NP_000175.1:n.93-33C>G