Canonical Allele Identifier: CA10158027

Gene: CRYBB2

Linked Data

• dbSNP Id: rs137852878
• ExAC: 22:25627539 C / G
• gnomAD v2: 22-25627539-C-G
• gnomAD v3: 22-25231572-C-G
• gnomAD v4: 22-25231572-C-G
• MyVariant Identifiers: chr22:g.25627539C>G (hg19) ; chr22:g.25231572C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.25231572C>G , CM000684.2:g.25231572C>G	GRCh38
NC_000022.10:g.25627539C>G , CM000684.1:g.25627539C>G	GRCh37
NC_000022.9:g.23957539C>G	NCBI36
NG_009827.1:g.16928C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398215.3:c.450-32C>G MANE Select	ENSP00000381273.2:n.450-32C>G
ENST00000651629.1:c.450-32C>G	ENSP00000498905.1:n.450-32C>G
ENST00000398215.2:c.450-32C>G	ENSP00000381273.2:n.450-32C>G
NM_000496.2:c.450-32C>G	NP_000487.1:n.450-32C>G
XM_006724141.2:c.450-32C>G	XP_006724204.1:n.450-32C>G
XM_011529900.1:c.450-32C>G	XP_011528202.1:n.450-32C>G
XM_011529901.1:c.450-32C>G	XP_011528203.1:n.450-32C>G
XM_006724141.3:c.450-32C>G	XP_006724204.1:n.450-32C>G
XM_011529900.2:c.450-32C>G	XP_011528202.1:n.450-32C>G
NM_000496.3:c.450-32C>G MANE Select	NP_000487.1:n.450-32C>G