Canonical Allele Identifier: CA13688532

Gene: RBMS2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56544599T>G , CM000674.2:g.56544599T>G	GRCh38
NC_000012.11:g.56938383T>G , CM000674.1:g.56938383T>G	GRCh37
NC_000012.10:g.55224650T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262031.10:c.67-17818T>G MANE Select	ENSP00000262031.5:n.67-17818T>G
ENST00000262031.9:c.67-17818T>G	ENSP00000262031.5:n.67-17818T>G
ENST00000542360.1:c.-143+22510T>G	ENSP00000443486.1:n.-143+22510T>G
ENST00000549945.5:n.194+16636T>G
ENST00000550726.5:c.-143+22510T>G	ENSP00000449678.1:n.-143+22510T>G
ENST00000551369.5:c.145+4835T>G	ENSP00000447699.1:n.145+4835T>G
ENST00000552247.6:c.67-17818T>G	ENSP00000447426.1:n.67-17818T>G
ENST00000552916.5:c.67-17818T>G	ENSP00000450127.1:n.67-17818T>G
NM_002898.3:c.67-17818T>G	NP_002889.1:n.67-17818T>G
XM_005269059.3:c.67-17818T>G	XP_005269116.1:n.67-17818T>G
XM_005269060.3:c.67-17818T>G	XP_005269117.1:n.67-17818T>G
XM_005269061.2:c.67-17818T>G	XP_005269118.1:n.67-17818T>G
XM_005269066.3:c.67-17818T>G	XP_005269123.1:n.67-17818T>G
XM_006719541.2:c.67-17818T>G	XP_006719604.1:n.67-17818T>G
XM_006719542.2:c.67-17818T>G	XP_006719605.1:n.67-17818T>G
XM_006719543.2:c.67-17818T>G	XP_006719606.1:n.67-17818T>G
XM_006719544.2:c.67-17818T>G	XP_006719607.1:n.67-17818T>G
XM_011538637.1:c.9+2211T>G	XP_011536939.1:n.9+2211T>G
XM_011538638.1:c.-196-17818T>G	XP_011536940.1:n.-196-17818T>G
XM_011538639.1:c.67-17818T>G	XP_011536941.1:n.67-17818T>G
XM_011538640.1:c.67-17818T>G	XP_011536942.1:n.67-17818T>G
XM_005269059.5:c.67-17818T>G	XP_005269116.1:n.67-17818T>G
XM_005269060.5:c.67-17818T>G	XP_005269117.1:n.67-17818T>G
XM_005269061.3:c.67-17818T>G	XP_005269118.1:n.67-17818T>G
XM_005269066.4:c.67-17818T>G	XP_005269123.1:n.67-17818T>G
XM_006719541.4:c.67-17818T>G	XP_006719604.1:n.67-17818T>G
XM_006719542.4:c.67-17818T>G	XP_006719605.1:n.67-17818T>G
XM_006719543.4:c.67-17818T>G	XP_006719606.1:n.67-17818T>G
XM_006719544.4:c.67-17818T>G	XP_006719607.1:n.67-17818T>G
XM_011538637.3:c.9+2211T>G	XP_011536939.1:n.9+2211T>G
XM_011538638.3:c.-196-17818T>G	XP_011536940.1:n.-196-17818T>G
XM_011538639.2:c.67-17818T>G	XP_011536941.1:n.67-17818T>G
XM_011538640.3:c.67-17818T>G	XP_011536942.1:n.67-17818T>G
XM_017019775.2:c.9+2211T>G	XP_016875264.1:n.9+2211T>G
XM_024449115.1:c.-24-17818T>G	XP_024304883.1:n.-24-17818T>G
XM_024449117.1:c.-24-17818T>G	XP_024304885.1:n.-24-17818T>G
XR_002957368.1:n.134-17818T>G
NM_002898.4:c.67-17818T>G MANE Select	NP_002889.1:n.67-17818T>G