Canonical Allele Identifier: CA751955518

Gene: CRYBB2

Linked Data

• dbSNP Id: rs1381907535
• gnomAD v3: 22-25231819-A-G
• gnomAD v4: 22-25231819-A-G
• MyVariant Identifiers: chr22:g.25627786A>G (hg19) ; chr22:g.25231819A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.25231819A>G , CM000684.2:g.25231819A>G	GRCh38
NC_000022.10:g.25627786A>G , CM000684.1:g.25627786A>G	GRCh37
NC_000022.9:g.23957786A>G	NCBI36
NG_009827.1:g.17175A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398215.3:c.*47A>G MANE Select	ENSP00000381273.2:n.*47A>G
ENST00000651629.1:c.*47A>G	ENSP00000498905.1:n.*47A>G
ENST00000398215.2:c.*47A>G	ENSP00000381273.2:n.*47A>G
NM_000496.2:c.*47A>G	NP_000487.1:n.*47A>G
XM_006724141.2:c.*47A>G	XP_006724204.1:n.*47A>G
XM_011529900.1:c.*47A>G	XP_011528202.1:n.*47A>G
XM_011529901.1:c.*47A>G	XP_011528203.1:n.*47A>G
XM_006724141.3:c.*47A>G	XP_006724204.1:n.*47A>G
XM_011529900.2:c.*47A>G	XP_011528202.1:n.*47A>G
NM_000496.3:c.*47A>G MANE Select	NP_000487.1:n.*47A>G