Canonical Allele Identifier: CA2612151133
Gene: HBG2 HGNC NCBI

Linked Data

gnomAD v4: 11-5253104-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5253104A>C , CM000673.2:g.5253104A>C GRCh38
NC_000011.9:g.5274334A>C , CM000673.1:g.5274334A>C GRCh37
NC_000011.8:g.5230910A>C NCBI36
NG_000007.3:g.44512T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.315+1188T>G ENSP00000495346.1:n.315+1188T>G
ENST00000647543.1:c.378+239T>G ENSP00000496470.1:n.378+239T>G
ENST00000620888.4:c.315+1188T>G ENSP00000479637.1:n.315+1188T>G