Canonical Allele Identifier: CA1558747075
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs1755516186

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206744C>T , CM000667.2:g.81206744C>T GRCh38
NC_000005.9:g.80502563C>T , CM000667.1:g.80502563C>T GRCh37
NC_000005.8:g.80538319C>T NCBI36
NG_030334.1:g.251056C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2907-101C>T MANE Select ENSP00000265080.4:n.2907-101C>T
ENST00000265080.8:c.2907-101C>T ENSP00000265080.4:n.2907-101C>T
ENST00000503795.1:c.2907-101C>T ENSP00000421771.1:n.2907-101C>T
NM_006909.2:c.2907-101C>T NP_008840.1:n.2907-101C>T
XM_017009682.2:c.2622-101C>T XP_016865171.1:n.2622-101C>T
XR_002956166.1:n.3023-101C>T
NM_006909.3:c.2907-101C>T MANE Select NP_008840.1:n.2907-101C>T