Canonical Allele Identifier: CA2580980470
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226496G>C , CM000673.2:g.5226496G>C GRCh38
NC_000011.9:g.5247726G>C , CM000673.1:g.5247726G>C GRCh37
NC_000011.8:g.5204302G>C NCBI36
NG_000007.3:g.71120C>G
NG_059281.1:g.5576C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.315+81C>G ENSP00000494175.1:n.315+81C>G
ENST00000335295.4:c.315+81C>G MANE Select ENSP00000333994.3:n.315+81C>G
ENST00000475226.1:n.247+81C>G
ENST00000485743.1:n.447C>G
ENST00000633227.1:c.*131+81C>G ENSP00000488004.1:n.*131+81C>G
NM_000518.4:c.315+81C>G NP_000509.1:n.315+81C>G
NM_000518.5:c.315+81C>G MANE Select NP_000509.1:n.315+81C>G