Canonical Allele Identifier: CA2695213000
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225629_5225632del , CM000673.2:g.5225629_5225632del GRCh38
NC_000011.9:g.5246859_5246862del , CM000673.1:g.5246859_5246862del GRCh37
NC_000011.8:g.5203435_5203438del NCBI36
NG_000007.3:g.71985_71988del
NG_059281.1:g.6441_6444del

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.411_414del ENSP00000494175.1:p.Val138LeufsTer20
ENST00000335295.4:c.411_414del MANE Select ENSP00000333994.3:p.Val138LeufsTer20
ENST00000633227.1:c.*227_*230del ENSP00000488004.1:n.*227_*230del
NM_000518.4:c.411_414del NP_000509.1:p.Val138LeufsTer20
NM_000518.5:c.411_414del MANE Select NP_000509.1:p.Val138LeufsTer20