Canonical Allele Identifier: CA2767192818
Gene: RASGRF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207214G>C , CM000667.2:g.81207214G>C GRCh38
NC_000005.9:g.80503033G>C , CM000667.1:g.80503033G>C GRCh37
NC_000005.8:g.80538789G>C NCBI36
NG_030334.1:g.251526G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2968-32G>C MANE Select ENSP00000265080.4:n.2968-32G>C
ENST00000265080.8:c.2968-32G>C ENSP00000265080.4:n.2968-32G>C
ENST00000503795.1:c.2968-32G>C ENSP00000421771.1:n.2968-32G>C
NM_006909.2:c.2968-32G>C NP_008840.1:n.2968-32G>C
XM_017009682.2:c.2683-32G>C XP_016865171.1:n.2683-32G>C
XR_002956166.1:n.3084-32G>C
NM_006909.3:c.2968-32G>C MANE Select NP_008840.1:n.2968-32G>C