Canonical Allele Identifier: CA360289586
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs1354541680
gnomAD v3: 5-81206865-A-G
gnomAD v4: 5-81206865-A-G
MyVariant Identifiers: chr5:g.80502684A>G (hg19) chr5:g.81206865A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206865A>G , CM000667.2:g.81206865A>G GRCh38
NC_000005.9:g.80502684A>G , CM000667.1:g.80502684A>G GRCh37
NC_000005.8:g.80538440A>G NCBI36
NG_030334.1:g.251177A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2927A>G MANE Select ENSP00000265080.4:p.Gln976Arg
ENST00000265080.8:c.2927A>G ENSP00000265080.4:p.Gln976Arg
ENST00000503795.1:c.2927A>G ENSP00000421771.1:p.Gln976Arg
NM_006909.2:c.2927A>G NP_008840.1:p.Gln976Arg
XM_017009682.2:c.2642A>G XP_016865171.1:p.Gln881Arg
XR_002956166.1:n.3043A>G
NM_006909.3:c.2927A>G MANE Select NP_008840.1:p.Gln976Arg
Search 100 bp 5'
Search 100 bp 3'