Canonical Allele Identifier: CA379273768
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226590G>T , CM000673.2:g.5226590G>T GRCh38
NC_000011.9:g.5247820G>T , CM000673.1:g.5247820G>T GRCh37
NC_000011.8:g.5204396G>T NCBI36
NG_000007.3:g.71026C>A
NG_059281.1:g.5482C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.302C>A ENSP00000494175.1:p.Pro101His
ENST00000335295.4:c.302C>A MANE Select ENSP00000333994.3:p.Pro101His
ENST00000475226.1:n.234C>A
ENST00000485743.1:n.353C>A
ENST00000633227.1:c.*118C>A ENSP00000488004.1:n.*118C>A
NM_000518.4:c.302C>A NP_000509.1:p.Pro101His
NM_000518.5:c.302C>A MANE Select NP_000509.1:p.Pro101His