Canonical Allele Identifier: CA814488466
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs1269414138
gnomAD v3: 5-81207001-A-G
gnomAD v4: 5-81207001-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207001A>G , CM000667.2:g.81207001A>G GRCh38
NC_000005.9:g.80502820A>G , CM000667.1:g.80502820A>G GRCh37
NC_000005.8:g.80538576A>G NCBI36
NG_030334.1:g.251313A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2967+96A>G MANE Select ENSP00000265080.4:n.2967+96A>G
ENST00000265080.8:c.2967+96A>G ENSP00000265080.4:n.2967+96A>G
ENST00000503795.1:c.2967+96A>G ENSP00000421771.1:n.2967+96A>G
NM_006909.2:c.2967+96A>G NP_008840.1:n.2967+96A>G
XM_017009682.2:c.2682+96A>G XP_016865171.1:n.2682+96A>G
XR_002956166.1:n.3083+96A>G
NM_006909.3:c.2967+96A>G MANE Select NP_008840.1:n.2967+96A>G