Canonical Allele Identifier: CA445167060

Gene: RASGRF2

Linked Data

• MyVariant Identifiers: chr5:g.80503067T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81207248T>C , CM000667.2:g.81207248T>C	GRCh38
NC_000005.9:g.80503067T>C , CM000667.1:g.80503067T>C	GRCh37
NC_000005.8:g.80538823T>C	NCBI36
NG_030334.1:g.251560T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265080.9:c.2970T>C MANE Select	ENSP00000265080.4:p.Thr990=
ENST00000265080.8:c.2970T>C	ENSP00000265080.4:p.Thr990=
ENST00000503795.1:c.2970T>C	ENSP00000421771.1:p.Thr990=
NM_006909.2:c.2970T>C	NP_008840.1:p.Thr990=
XM_017009682.2:c.2685T>C	XP_016865171.1:p.Thr895=
XR_002956166.1:n.3086T>C
NM_006909.3:c.2970T>C MANE Select	NP_008840.1:p.Thr990=