Canonical Allele Identifier: CA638953143

Gene: CRYBB2

Linked Data

• dbSNP Id: rs1249277466
• gnomAD v2: 22-25627532-T-C
• gnomAD v4: 22-25231565-T-C
• MyVariant Identifiers: chr22:g.25627532T>C (hg19) ; chr22:g.25231565T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.25231565T>C , CM000684.2:g.25231565T>C	GRCh38
NC_000022.10:g.25627532T>C , CM000684.1:g.25627532T>C	GRCh37
NC_000022.9:g.23957532T>C	NCBI36
NG_009827.1:g.16921T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398215.3:c.450-39T>C MANE Select	ENSP00000381273.2:n.450-39T>C
ENST00000651629.1:c.450-39T>C	ENSP00000498905.1:n.450-39T>C
ENST00000398215.2:c.450-39T>C	ENSP00000381273.2:n.450-39T>C
NM_000496.2:c.450-39T>C	NP_000487.1:n.450-39T>C
XM_006724141.2:c.450-39T>C	XP_006724204.1:n.450-39T>C
XM_011529900.1:c.450-39T>C	XP_011528202.1:n.450-39T>C
XM_011529901.1:c.450-39T>C	XP_011528203.1:n.450-39T>C
XM_006724141.3:c.450-39T>C	XP_006724204.1:n.450-39T>C
XM_011529900.2:c.450-39T>C	XP_011528202.1:n.450-39T>C
NM_000496.3:c.450-39T>C MANE Select	NP_000487.1:n.450-39T>C