Canonical Allele Identifier: CA916083199
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 869222
ClinVar RCV Id: RCV001078249
dbSNP Id: rs1847560327

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226722_5226723insACCTTAGGGTTGCC , CM000673.2:g.5226722_5226723insACCTTAGGGTTGCC GRCh38
NC_000011.9:g.5247952_5247953insACCTTAGGGTTGCC , CM000673.1:g.5247952_5247953insACCTTAGGGTTGCC GRCh37
NC_000011.8:g.5204528_5204529insACCTTAGGGTTGCC NCBI36
NG_000007.3:g.70894_70895insGCAACCCTAAGGTG
NG_059281.1:g.5350_5351insGCAACCCTAAGGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.170_171insGCAACCCTAAGGTG ENSP00000494175.1:p.Asn58GlnfsTer3
ENST00000335295.4:c.170_171insGCAACCCTAAGGTG MANE Select ENSP00000333994.3:p.Asn58GlnfsTer3
ENST00000380315.2:c.170_171insGCAACCCTAAGGTG ENSP00000369671.2:p.Asn58GlnfsTer3
ENST00000475226.1:n.102_103insGCAACCCTAAGGTG
ENST00000485743.1:n.221_222insGCAACCCTAAGGTG
ENST00000633227.1:c.154_155insGCAACCCTAAGGTG ENSP00000488004.1:p.Ala52GlyfsTer8
NM_000518.4:c.170_171insGCAACCCTAAGGTG NP_000509.1:p.Asn58GlnfsTer3
NM_000518.5:c.170_171insGCAACCCTAAGGTG MANE Select NP_000509.1:p.Asn58GlnfsTer3