Canonical Allele Identifier: CA2612162208
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225536dup , CM000673.2:g.5225536dup GRCh38
NC_000011.9:g.5246766dup , CM000673.1:g.5246766dup GRCh37
NC_000011.8:g.5203342dup NCBI36
NG_000007.3:g.72082dup
NG_059281.1:g.6538dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*64dup ENSP00000494175.1:n.*64dup
ENST00000335295.4:c.*64dup MANE Select ENSP00000333994.3:n.*64dup
ENST00000633227.1:c.*324dup ENSP00000488004.1:n.*324dup
NM_000518.4:c.*64dup NP_000509.1:n.*64dup
NM_000518.5:c.*64dup MANE Select NP_000509.1:n.*64dup