Canonical Allele Identifier: CA1949565707
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225824_5225825delinsGA , CM000673.2:g.5225824_5225825delinsGA GRCh38
NC_000011.9:g.5247054_5247055delinsGA , CM000673.1:g.5247054_5247055delinsGA GRCh37
NC_000011.8:g.5203630_5203631delinsGA NCBI36
NG_000007.3:g.71791_71792delinsTC
NG_059281.1:g.6247_6248delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.316-99_316-98delinsTC ENSP00000494175.1:n.316-99_316-98delinsTC
ENST00000335295.4:c.316-99_316-98delinsTC MANE Select ENSP00000333994.3:n.316-99_316-98delinsTC
ENST00000475226.1:n.248-99_248-98delinsTC
ENST00000633227.1:c.*132-99_*132-98delinsTC ENSP00000488004.1:n.*132-99_*132-98delinsTC
NM_000518.4:c.316-99_316-98delinsTC NP_000509.1:n.316-99_316-98delinsTC
NM_000518.5:c.316-99_316-98delinsTC MANE Select NP_000509.1:n.316-99_316-98delinsTC