Canonical Allele Identifier: CA121361144

Gene: RASGRF2

Linked Data

• dbSNP Id: rs567665030
• gnomAD v3: 5-81207101-T-G
• gnomAD v4: 5-81207101-T-G
• MyVariant Identifiers: chr5:g.80502920T>G (hg19) ; chr5:g.81207101T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81207101T>G , CM000667.2:g.81207101T>G	GRCh38
NC_000005.9:g.80502920T>G , CM000667.1:g.80502920T>G	GRCh37
NC_000005.8:g.80538676T>G	NCBI36
NG_030334.1:g.251413T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265080.9:c.2968-145T>G MANE Select	ENSP00000265080.4:n.2968-145T>G
ENST00000265080.8:c.2968-145T>G	ENSP00000265080.4:n.2968-145T>G
ENST00000503795.1:c.2968-145T>G	ENSP00000421771.1:n.2968-145T>G
NM_006909.2:c.2968-145T>G	NP_008840.1:n.2968-145T>G
XM_017009682.2:c.2683-145T>G	XP_016865171.1:n.2683-145T>G
XR_002956166.1:n.3084-145T>G
NM_006909.3:c.2968-145T>G MANE Select	NP_008840.1:n.2968-145T>G