Canonical Allele Identifier: CA2579829634

Gene: HBG2

Linked Data

• gnomAD v4: 11-5249898-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249898T>G , CM000673.2:g.5249898T>G	GRCh38
NC_000011.9:g.5271128T>G , CM000673.1:g.5271128T>G	GRCh37
NC_000011.8:g.5227704T>G	NCBI36
NG_000007.3:g.47718A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642908.1:c.316-1411A>C	ENSP00000495346.1:n.316-1411A>C
ENST00000647543.1:c.379-1411A>C	ENSP00000496470.1:n.379-1411A>C
ENST00000620888.4:c.316-1411A>C	ENSP00000479637.1:n.316-1411A>C