Canonical Allele Identifier: CA121344662
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs138206701
gnomAD v2: 5-80406566-A-G
gnomAD v3: 5-81110747-A-G
gnomAD v4: 5-81110747-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81110747A>G , CM000667.2:g.81110747A>G GRCh38
NC_000005.9:g.80406566A>G , CM000667.1:g.80406566A>G GRCh37
NC_000005.8:g.80442322A>G NCBI36
NG_030334.1:g.155059A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.1838+1669A>G MANE Select ENSP00000265080.4:n.1838+1669A>G
ENST00000265080.8:c.1838+1669A>G ENSP00000265080.4:n.1838+1669A>G
ENST00000503795.1:c.1838+1669A>G ENSP00000421771.1:n.1838+1669A>G
NM_006909.2:c.1838+1669A>G NP_008840.1:n.1838+1669A>G
XM_005248565.1:c.1838+1669A>G XP_005248622.1:n.1838+1669A>G
XM_017009682.2:c.1553+1669A>G XP_016865171.1:n.1553+1669A>G
XM_017009683.1:c.1838+1669A>G XP_016865172.1:n.1838+1669A>G
XM_024446141.1:c.1838+1669A>G XP_024301909.1:n.1838+1669A>G
XR_002956166.1:n.1905+1669A>G
NM_006909.3:c.1838+1669A>G MANE Select NP_008840.1:n.1838+1669A>G