Canonical Allele Identifier: CA2695213051
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226735_5226741dup , CM000673.2:g.5226735_5226741dup GRCh38
NC_000011.9:g.5247965_5247971dup , CM000673.1:g.5247965_5247971dup GRCh37
NC_000011.8:g.5204541_5204547dup NCBI36
NG_000007.3:g.70876_70882dup
NG_059281.1:g.5332_5338dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.152_158dup ENSP00000494175.1:p.Ala54SerfsTer2
ENST00000335295.4:c.152_158dup MANE Select ENSP00000333994.3:p.Ala54SerfsTer2
ENST00000380315.2:c.152_158dup ENSP00000369671.2:p.Ala54SerfsTer2
ENST00000475226.1:n.84_90dup
ENST00000485743.1:n.203_209dup
ENST00000633227.1:c.136_142dup ENSP00000488004.1:p.Met48ThrfsTer?
NM_000518.4:c.152_158dup NP_000509.1:p.Ala54SerfsTer2
NM_000518.5:c.152_158dup MANE Select NP_000509.1:p.Ala54SerfsTer2