Canonical Allele Identifier: CA217113752
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs33991993

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226643C>A , CM000673.2:g.5226643C>A GRCh38
NC_000011.9:g.5247873C>A , CM000673.1:g.5247873C>A GRCh37
NC_000011.8:g.5204449C>A NCBI36
NG_000007.3:g.70973G>T
NG_059281.1:g.5429G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.249G>T ENSP00000494175.1:p.Lys83Asn
ENST00000335295.4:c.249G>T MANE Select ENSP00000333994.3:p.Lys83Asn
ENST00000380315.2:c.249G>T ENSP00000369671.2:p.Lys83Asn
ENST00000475226.1:n.181G>T
ENST00000485743.1:n.300G>T
ENST00000633227.1:c.*65G>T ENSP00000488004.1:n.*65G>T
NM_000518.4:c.249G>T NP_000509.1:p.Lys83Asn
NM_000518.5:c.249G>T MANE Select NP_000509.1:p.Lys83Asn