Canonical Allele Identifier: CA560571174
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs1377785753

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207121dup , CM000667.2:g.81207121dup GRCh38
NC_000005.9:g.80502940dup , CM000667.1:g.80502940dup GRCh37
NC_000005.8:g.80538696dup NCBI36
NG_030334.1:g.251433dup

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.2968-125dup MANE Select ENSP00000265080.4:n.2968-125dup
ENST00000265080.8:c.2968-125dup ENSP00000265080.4:n.2968-125dup
ENST00000503795.1:c.2968-125dup ENSP00000421771.1:n.2968-125dup
NM_006909.2:c.2968-125dup NP_008840.1:n.2968-125dup
XM_017009682.2:c.2683-125dup XP_016865171.1:n.2683-125dup
XR_002956166.1:n.3084-125dup
NM_006909.3:c.2968-125dup MANE Select NP_008840.1:n.2968-125dup