Canonical Allele Identifier: CA751955569
Gene: CRYBB2 HGNC NCBI

Linked Data

dbSNP Id: rs1368279772
gnomAD v3: 22-25231869-G-A
gnomAD v4: 22-25231869-G-A
MyVariant Identifiers: chr22:g.25627836G>A (hg19) chr22:g.25231869G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.25231869G>A , CM000684.2:g.25231869G>A GRCh38
NC_000022.10:g.25627836G>A , CM000684.1:g.25627836G>A GRCh37
NC_000022.9:g.23957836G>A NCBI36
NG_009827.1:g.17225G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398215.3:c.*97G>A MANE Select ENSP00000381273.2:n.*97G>A
ENST00000651629.1:c.*97G>A ENSP00000498905.1:n.*97G>A
ENST00000398215.2:c.*97G>A ENSP00000381273.2:n.*97G>A
NM_000496.2:c.*97G>A NP_000487.1:n.*97G>A
XM_006724141.2:c.*97G>A XP_006724204.1:n.*97G>A
XM_011529900.1:c.*97G>A XP_011528202.1:n.*97G>A
XM_011529901.1:c.*97G>A XP_011528203.1:n.*97G>A
XM_006724141.3:c.*97G>A XP_006724204.1:n.*97G>A
XM_011529900.2:c.*97G>A XP_011528202.1:n.*97G>A
NM_000496.3:c.*97G>A MANE Select NP_000487.1:n.*97G>A
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