Canonical Allele Identifier: CA1558747128
Gene: RASGRF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206866A= , CM000667.2:g.81206866A= GRCh38
NC_000005.9:g.80502685A= , CM000667.1:g.80502685A= GRCh37
NC_000005.8:g.80538441A= NCBI36
NG_030334.1:g.251178A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2928A= MANE Select ENSP00000265080.4:p.Gln976=
ENST00000265080.8:c.2928A= ENSP00000265080.4:p.Gln976=
ENST00000503795.1:c.2928A= ENSP00000421771.1:p.Gln976=
NM_006909.2:c.2928A= NP_008840.1:p.Gln976=
XM_017009682.2:c.2643A= XP_016865171.1:p.Gln881=
XR_002956166.1:n.3044A=
NM_006909.3:c.2928A= MANE Select NP_008840.1:p.Gln976=