Canonical Allele Identifier: CA379273662
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225629A>C , CM000673.2:g.5225629A>C GRCh38
NC_000011.9:g.5246859A>C , CM000673.1:g.5246859A>C GRCh37
NC_000011.8:g.5203435A>C NCBI36
NG_000007.3:g.71987T>G
NG_059281.1:g.6443T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.413T>G ENSP00000494175.1:p.Val138Gly
ENST00000335295.4:c.413T>G MANE Select ENSP00000333994.3:p.Val138Gly
ENST00000633227.1:c.*229T>G ENSP00000488004.1:n.*229T>G
NM_000518.4:c.413T>G NP_000509.1:p.Val138Gly
NM_000518.5:c.413T>G MANE Select NP_000509.1:p.Val138Gly