Canonical Allele Identifier: CA379273912
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226726T>C , CM000673.2:g.5226726T>C GRCh38
NC_000011.9:g.5247956T>C , CM000673.1:g.5247956T>C GRCh37
NC_000011.8:g.5204532T>C NCBI36
NG_000007.3:g.70890A>G
NG_059281.1:g.5346A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.166A>G ENSP00000494175.1:p.Met56Val
ENST00000335295.4:c.166A>G MANE Select ENSP00000333994.3:p.Met56Val
ENST00000380315.2:c.166A>G ENSP00000369671.2:p.Met56Val
ENST00000475226.1:n.98A>G
ENST00000485743.1:n.217A>G
ENST00000633227.1:c.150A>G ENSP00000488004.1:p.Leu50=
NM_000518.4:c.166A>G NP_000509.1:p.Met56Val
NM_000518.5:c.166A>G MANE Select NP_000509.1:p.Met56Val