Canonical Allele Identifier: CA1558747189
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs1755523136
gnomAD v4: 5-81207015-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207015C>G , CM000667.2:g.81207015C>G GRCh38
NC_000005.9:g.80502834C>G , CM000667.1:g.80502834C>G GRCh37
NC_000005.8:g.80538590C>G NCBI36
NG_030334.1:g.251327C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.2967+110C>G MANE Select ENSP00000265080.4:n.2967+110C>G
ENST00000265080.8:c.2967+110C>G ENSP00000265080.4:n.2967+110C>G
ENST00000503795.1:c.2967+110C>G ENSP00000421771.1:n.2967+110C>G
NM_006909.2:c.2967+110C>G NP_008840.1:n.2967+110C>G
XM_017009682.2:c.2682+110C>G XP_016865171.1:n.2682+110C>G
XR_002956166.1:n.3083+110C>G
NM_006909.3:c.2967+110C>G MANE Select NP_008840.1:n.2967+110C>G