Canonical Allele Identifier: CA1558747131
Gene: RASGRF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206876C= , CM000667.2:g.81206876C= GRCh38
NC_000005.9:g.80502695C= , CM000667.1:g.80502695C= GRCh37
NC_000005.8:g.80538451C= NCBI36
NG_030334.1:g.251188C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2938C= MANE Select ENSP00000265080.4:p.His980=
ENST00000265080.8:c.2938C= ENSP00000265080.4:p.His980=
ENST00000503795.1:c.2938C= ENSP00000421771.1:p.His980=
NM_006909.2:c.2938C= NP_008840.1:p.His980=
XM_017009682.2:c.2653C= XP_016865171.1:p.His885=
XR_002956166.1:n.3054C=
NM_006909.3:c.2938C= MANE Select NP_008840.1:p.His980=