Canonical Allele Identifier: CA1558747087

Gene: RASGRF2

Linked Data

• dbSNP Id: rs1755517103

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81206766A>G , CM000667.2:g.81206766A>G	GRCh38
NC_000005.9:g.80502585A>G , CM000667.1:g.80502585A>G	GRCh37
NC_000005.8:g.80538341A>G	NCBI36
NG_030334.1:g.251078A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265080.9:c.2907-79A>G MANE Select	ENSP00000265080.4:n.2907-79A>G
ENST00000265080.8:c.2907-79A>G	ENSP00000265080.4:n.2907-79A>G
ENST00000503795.1:c.2907-79A>G	ENSP00000421771.1:n.2907-79A>G
NM_006909.2:c.2907-79A>G	NP_008840.1:n.2907-79A>G
XM_017009682.2:c.2622-79A>G	XP_016865171.1:n.2622-79A>G
XR_002956166.1:n.3023-79A>G
NM_006909.3:c.2907-79A>G MANE Select	NP_008840.1:n.2907-79A>G