Canonical Allele Identifier: CA2398639016
Gene: CRYBB2 HGNC NCBI

Linked Data

dbSNP Id: rs1920986919

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.25231812_25231813insGAGGGTT , CM000684.2:g.25231812_25231813insGAGGGTT GRCh38
NC_000022.10:g.25627779_25627780insGAGGGTT , CM000684.1:g.25627779_25627780insGAGGGTT GRCh37
NC_000022.9:g.23957779_23957780insGAGGGTT NCBI36
NG_009827.1:g.17168_17169insGAGGGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000398215.3:c.*40_*41insGAGGGTT MANE Select ENSP00000381273.2:n.*40_*41insGAGGGTT
ENST00000651629.1:c.*40_*41insGAGGGTT ENSP00000498905.1:n.*40_*41insGAGGGTT
ENST00000398215.2:c.*40_*41insGAGGGTT ENSP00000381273.2:n.*40_*41insGAGGGTT
NM_000496.2:c.*40_*41insGAGGGTT NP_000487.1:n.*40_*41insGAGGGTT
XM_006724141.2:c.*40_*41insGAGGGTT XP_006724204.1:n.*40_*41insGAGGGTT
XM_011529900.1:c.*40_*41insGAGGGTT XP_011528202.1:n.*40_*41insGAGGGTT
XM_011529901.1:c.*40_*41insGAGGGTT XP_011528203.1:n.*40_*41insGAGGGTT
XM_006724141.3:c.*40_*41insGAGGGTT XP_006724204.1:n.*40_*41insGAGGGTT
XM_011529900.2:c.*40_*41insGAGGGTT XP_011528202.1:n.*40_*41insGAGGGTT
NM_000496.3:c.*40_*41insGAGGGTT MANE Select NP_000487.1:n.*40_*41insGAGGGTT