Canonical Allele Identifier: CA217119009

Gene: HBG2

Linked Data

• dbSNP Id: rs63750509
• MyVariant Identifiers: chr11:g.5271189_5271201del (hg19) ; chr11:g.5249959_5249971del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249967_5249979del , CM000673.2:g.5249967_5249979del	GRCh38
NC_000011.9:g.5271197_5271209del , CM000673.1:g.5271197_5271209del	GRCh37
NC_000011.8:g.5227773_5227785del	NCBI36
NG_000007.3:g.47645_47657del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642908.1:c.316-1484_316-1472del	ENSP00000495346.1:n.316-1484_316-1472del
ENST00000647543.1:c.379-1484_379-1472del	ENSP00000496470.1:n.379-1484_379-1472del
ENST00000620888.4:c.316-1484_316-1472del	ENSP00000479637.1:n.316-1484_316-1472del