Canonical Allele Identifier: CA12030075

Gene: RASGRF2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81115402G>A , CM000667.2:g.81115402G>A	GRCh38
NC_000005.9:g.80411221G>A , CM000667.1:g.80411221G>A	GRCh37
NC_000005.8:g.80446977G>A	NCBI36
NG_030334.1:g.159714G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265080.9:c.2470+1482G>A MANE Select	ENSP00000265080.4:n.2470+1482G>A
ENST00000265080.8:c.2470+1482G>A	ENSP00000265080.4:n.2470+1482G>A
ENST00000503795.1:c.2470+1482G>A	ENSP00000421771.1:n.2470+1482G>A
NM_006909.2:c.2470+1482G>A	NP_008840.1:n.2470+1482G>A
XM_005248565.1:c.2470+1482G>A	XP_005248622.1:n.2470+1482G>A
XM_017009682.2:c.2185+1482G>A	XP_016865171.1:n.2185+1482G>A
XM_017009683.1:c.2470+1482G>A	XP_016865172.1:n.2470+1482G>A
XM_024446141.1:c.2470+1482G>A	XP_024301909.1:n.2470+1482G>A
XR_002956166.1:n.2537+1482G>A
NM_006909.3:c.2470+1482G>A MANE Select	NP_008840.1:n.2470+1482G>A