Canonical Allele Identifier: CA411035127

Gene: CRYBB1 CRYBA4

Linked Data

• ClinVar Variation Id: 900138
• ClinVar RCV Id: RCV001145133
• dbSNP Id: rs1929353737
• MyVariant Identifiers: chr22:g.27012271C>T (hg19) ; chr22:g.26616307C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26616307C>T , CM000684.2:g.26616307C>T	GRCh38
NC_000022.10:g.27012271C>T , CM000684.1:g.27012271C>T	GRCh37
NC_000022.9:g.25342271C>T	NCBI36
NG_009826.1:g.6721G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647684.1:c.13G>A (CRYBB1) MANE Select	ENSP00000497249.1:p.Ala5Thr
ENST00000215939.2:c.13G>A (CRYBB1)	ENSP00000215939.2:p.Ala5Thr
NM_001887.3:c.13G>A (CRYBB1)	NP_001878.1:p.Ala5Thr
XM_006724140.2:c.4-6278C>T (CRYBA4)	XP_006724203.1:n.4-6278C>T
XM_011529898.1:c.24-5601C>T (CRYBA4)	XP_011528200.1:n.24-5601C>T
XM_011529899.1:c.13G>A (CRYBB1)	XP_011528201.1:p.Ala5Thr
NM_001887.4:c.13G>A (CRYBB1) MANE Select	NP_001878.1:p.Ala5Thr
XM_006724140.3:c.4-6278C>T (CRYBA4)	XP_006724203.1:n.4-6278C>T
XM_011529899.3:c.13G>A (CRYBB1)	XP_011528201.1:p.Ala5Thr