Canonical Allele Identifier: CA1949568895
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226725_5226726delinsAT , CM000673.2:g.5226725_5226726delinsAT GRCh38
NC_000011.9:g.5247955_5247956delinsAT , CM000673.1:g.5247955_5247956delinsAT GRCh37
NC_000011.8:g.5204531_5204532delinsAT NCBI36
NG_000007.3:g.70890_70891delinsAT
NG_059281.1:g.5346_5347delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.166_167delinsAT ENSP00000494175.1:p.Met56=
ENST00000335295.4:c.166_167delinsAT MANE Select ENSP00000333994.3:p.Met56=
ENST00000380315.2:c.166_167delinsAT ENSP00000369671.2:p.Met56=
ENST00000475226.1:n.98_99delinsAT
ENST00000485743.1:n.217_218delinsAT
ENST00000633227.1:c.150_151delinsAT ENSP00000488004.1:p.Leu50=
NM_000518.4:c.166_167delinsAT NP_000509.1:p.Met56=
NM_000518.5:c.166_167delinsAT MANE Select NP_000509.1:p.Met56=