Canonical Allele Identifier: CA379264105

Gene: HBG2

Linked Data

• dbSNP Id: rs1847992131
• gnomAD v4: 11-5254306-G-A
• COSMIC: COSM927856
• MyVariant Identifiers: chr11:g.5275536G>A (hg19) ; chr11:g.5254306G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254306G>A , CM000673.2:g.5254306G>A	GRCh38
NC_000011.9:g.5275536G>A , CM000673.1:g.5275536G>A	GRCh37
NC_000011.8:g.5232112G>A	NCBI36
NG_000007.3:g.43310C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.301C>T MANE Select	ENSP00000338082.4:p.Pro101Ser
ENST00000380252.6:c.136C>T	ENSP00000369602.2:p.Pro46Ser
ENST00000642908.1:c.301C>T	ENSP00000495346.1:p.Pro101Ser
ENST00000647543.1:c.301C>T	ENSP00000496470.1:p.Pro101Ser
ENST00000336906.4:c.301C>T	ENSP00000338082.4:p.Pro101Ser
ENST00000380252.5:c.271C>T	ENSP00000369602.1:p.Pro91Ser
ENST00000380259.6:c.301C>T	ENSP00000369609.2:p.Pro101Ser
ENST00000444587.1:c.*170C>T	ENSP00000488218.1:n.*170C>T
ENST00000620888.4:c.301C>T	ENSP00000479637.1:p.Pro101Ser
ENST00000624109.1:c.54G>A	ENSP00000485458.1:p.Arg18=
NM_000184.2:c.301C>T	NP_000175.1:p.Pro101Ser
NM_000184.3:c.301C>T MANE Select	NP_000175.1:p.Pro101Ser