Canonical Allele Identifier: CA217112801
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs33958739

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225716T>C , CM000673.2:g.5225716T>C GRCh38
NC_000011.9:g.5246946T>C , CM000673.1:g.5246946T>C GRCh37
NC_000011.8:g.5203522T>C NCBI36
NG_000007.3:g.71900A>G
NG_059281.1:g.6356A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.326A>G ENSP00000494175.1:p.Asn109Ser
ENST00000335295.4:c.326A>G MANE Select ENSP00000333994.3:p.Asn109Ser
ENST00000475226.1:n.258A>G
ENST00000633227.1:c.*142A>G ENSP00000488004.1:n.*142A>G
NM_000518.4:c.326A>G NP_000509.1:p.Asn109Ser
NM_000518.5:c.326A>G MANE Select NP_000509.1:p.Asn109Ser