Canonical Allele Identifier: CA379273798
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226623C>A , CM000673.2:g.5226623C>A GRCh38
NC_000011.9:g.5247853C>A , CM000673.1:g.5247853C>A GRCh37
NC_000011.8:g.5204429C>A NCBI36
NG_000007.3:g.70993G>T
NG_059281.1:g.5449G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.269G>T ENSP00000494175.1:p.Ser90Ile
ENST00000335295.4:c.269G>T MANE Select ENSP00000333994.3:p.Ser90Ile
ENST00000380315.2:c.269G>T ENSP00000369671.2:p.Ser90Ile
ENST00000475226.1:n.201G>T
ENST00000485743.1:n.320G>T
ENST00000633227.1:c.*85G>T ENSP00000488004.1:n.*85G>T
NM_000518.4:c.269G>T NP_000509.1:p.Ser90Ile
NM_000518.5:c.269G>T MANE Select NP_000509.1:p.Ser90Ile