Canonical Allele Identifier: CA360289713

Gene: RASGRF2

Linked Data

• MyVariant Identifiers: chr5:g.80502718T>G (hg19) ; chr5:g.81206899T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81206899T>G , CM000667.2:g.81206899T>G	GRCh38
NC_000005.9:g.80502718T>G , CM000667.1:g.80502718T>G	GRCh37
NC_000005.8:g.80538474T>G	NCBI36
NG_030334.1:g.251211T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265080.9:c.2961T>G MANE Select	ENSP00000265080.4:p.Ile987Met
ENST00000265080.8:c.2961T>G	ENSP00000265080.4:p.Ile987Met
ENST00000503795.1:c.2961T>G	ENSP00000421771.1:p.Ile987Met
NM_006909.2:c.2961T>G	NP_008840.1:p.Ile987Met
XM_017009682.2:c.2676T>G	XP_016865171.1:p.Ile892Met
XR_002956166.1:n.3077T>G
NM_006909.3:c.2961T>G MANE Select	NP_008840.1:p.Ile987Met