Canonical Allele Identifier: CA379273739
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225710A>C , CM000673.2:g.5225710A>C GRCh38
NC_000011.9:g.5246940A>C , CM000673.1:g.5246940A>C GRCh37
NC_000011.8:g.5203516A>C NCBI36
NG_000007.3:g.71906T>G
NG_059281.1:g.6362T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.332T>G ENSP00000494175.1:p.Leu111Arg
ENST00000335295.4:c.332T>G MANE Select ENSP00000333994.3:p.Leu111Arg
ENST00000475226.1:n.264T>G
ENST00000633227.1:c.*148T>G ENSP00000488004.1:n.*148T>G
NM_000518.4:c.332T>G NP_000509.1:p.Leu111Arg
NM_000518.5:c.332T>G MANE Select NP_000509.1:p.Leu111Arg