Canonical Allele Identifier: CA2612162202
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225530_5225531insA , CM000673.2:g.5225530_5225531insA GRCh38
NC_000011.9:g.5246760_5246761insA , CM000673.1:g.5246760_5246761insA GRCh37
NC_000011.8:g.5203336_5203337insA NCBI36
NG_000007.3:g.72085_72086insT
NG_059281.1:g.6541_6542insT

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*67_*68insT ENSP00000494175.1:n.*67_*68insT
ENST00000335295.4:c.*67_*68insT MANE Select ENSP00000333994.3:n.*67_*68insT
ENST00000633227.1:c.*327_*328insT ENSP00000488004.1:n.*327_*328insT
NM_000518.4:c.*67_*68insT NP_000509.1:n.*67_*68insT
NM_000518.5:c.*67_*68insT MANE Select NP_000509.1:n.*67_*68insT