Canonical Allele Identifier: CA360289978

Gene: RASGRF2

Linked Data

• MyVariant Identifiers: chr5:g.80503116G>T (hg19) ; chr5:g.81207297G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81207297G>T , CM000667.2:g.81207297G>T	GRCh38
NC_000005.9:g.80503116G>T , CM000667.1:g.80503116G>T	GRCh37
NC_000005.8:g.80538872G>T	NCBI36
NG_030334.1:g.251609G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265080.9:c.3019G>T MANE Select	ENSP00000265080.4:p.Ala1007Ser
ENST00000265080.8:c.3019G>T	ENSP00000265080.4:p.Ala1007Ser
ENST00000503795.1:c.3019G>T	ENSP00000421771.1:p.Ala1007Ser
NM_006909.2:c.3019G>T	NP_008840.1:p.Ala1007Ser
XM_017009682.2:c.2734G>T	XP_016865171.1:p.Ala912Ser
XR_002956166.1:n.3135G>T
NM_006909.3:c.3019G>T MANE Select	NP_008840.1:p.Ala1007Ser