Canonical Allele Identifier: CA1558747188
Gene: RASGRF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207015C= , CM000667.2:g.81207015C= GRCh38
NC_000005.9:g.80502834C= , CM000667.1:g.80502834C= GRCh37
NC_000005.8:g.80538590C= NCBI36
NG_030334.1:g.251327C=

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.2967+110C= MANE Select ENSP00000265080.4:n.2967+110C=
ENST00000265080.8:c.2967+110C= ENSP00000265080.4:n.2967+110C=
ENST00000503795.1:c.2967+110C= ENSP00000421771.1:n.2967+110C=
NM_006909.2:c.2967+110C= NP_008840.1:n.2967+110C=
XM_017009682.2:c.2682+110C= XP_016865171.1:n.2682+110C=
XR_002956166.1:n.3083+110C=
NM_006909.3:c.2967+110C= MANE Select NP_008840.1:n.2967+110C=