Canonical Allele Identifier: CA121361174

Gene: RASGRF2

Linked Data

• dbSNP Id: rs1038076250
• gnomAD v2: 5-80502988-G-A
• gnomAD v3: 5-81207169-G-A
• gnomAD v4: 5-81207169-G-A
• MyVariant Identifiers: chr5:g.80502988G>A (hg19) ; chr5:g.81207169G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81207169G>A , CM000667.2:g.81207169G>A	GRCh38
NC_000005.9:g.80502988G>A , CM000667.1:g.80502988G>A	GRCh37
NC_000005.8:g.80538744G>A	NCBI36
NG_030334.1:g.251481G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265080.9:c.2968-77G>A MANE Select	ENSP00000265080.4:n.2968-77G>A
ENST00000265080.8:c.2968-77G>A	ENSP00000265080.4:n.2968-77G>A
ENST00000503795.1:c.2968-77G>A	ENSP00000421771.1:n.2968-77G>A
NM_006909.2:c.2968-77G>A	NP_008840.1:n.2968-77G>A
XM_017009682.2:c.2683-77G>A	XP_016865171.1:n.2683-77G>A
XR_002956166.1:n.3084-77G>A
NM_006909.3:c.2968-77G>A MANE Select	NP_008840.1:n.2968-77G>A