Canonical Allele Identifier: CA245095821

Gene: KSR2

Linked Data

• dbSNP Id: rs570759945
• gnomAD v3: 12-117916095-T-C
• gnomAD v4: 12-117916095-T-C
• MyVariant Identifiers: chr12:g.118353900T>C (hg19) ; chr12:g.117916095T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117916095T>C , CM000674.2:g.117916095T>C	GRCh38
NC_000012.11:g.118353900T>C , CM000674.1:g.118353900T>C	GRCh37
NC_000012.10:g.116838283T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000339824.7:c.180+51981A>G MANE Select	ENSP00000339952.4:n.180+51981A>G
ENST00000339824.6:c.180+51981A>G	ENSP00000339952.4:n.180+51981A>G
ENST00000425217.5:c.93+51981A>G	ENSP00000389715.1:n.93+51981A>G
NM_173598.4:c.93+51981A>G	NP_775869.3:n.93+51981A>G
XM_011538224.1:c.180+51981A>G	XP_011536526.1:n.180+51981A>G
XM_011538226.1:c.180+51981A>G	XP_011536528.1:n.180+51981A>G
XM_011538229.1:c.180+51981A>G	XP_011536531.1:n.180+51981A>G
XR_944522.1:n.1014+51981A>G
XM_011538224.3:c.180+51981A>G	XP_011536526.1:n.180+51981A>G
XM_011538226.3:c.180+51981A>G	XP_011536528.1:n.180+51981A>G
XM_011538229.3:c.180+51981A>G	XP_011536531.1:n.180+51981A>G
XM_017019208.2:c.180+51981A>G	XP_016874697.1:n.180+51981A>G
XM_017019209.2:c.180+51981A>G	XP_016874698.1:n.180+51981A>G
NM_173598.6:c.180+51981A>G MANE Select	NP_775869.4:n.180+51981A>G