Canonical Allele Identifier: CA1558747120
Gene: RASGRF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206846G= , CM000667.2:g.81206846G= GRCh38
NC_000005.9:g.80502665G= , CM000667.1:g.80502665G= GRCh37
NC_000005.8:g.80538421G= NCBI36
NG_030334.1:g.251158G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2908G= MANE Select ENSP00000265080.4:p.Ala970=
ENST00000265080.8:c.2908G= ENSP00000265080.4:p.Ala970=
ENST00000503795.1:c.2908G= ENSP00000421771.1:p.Ala970=
NM_006909.2:c.2908G= NP_008840.1:p.Ala970=
XM_017009682.2:c.2623G= XP_016865171.1:p.Ala875=
XR_002956166.1:n.3024G=
NM_006909.3:c.2908G= MANE Select NP_008840.1:p.Ala970=