Canonical Allele Identifier: CA121361127

Gene: RASGRF2

Linked Data

• dbSNP Id: rs779358535
• gnomAD v2: 5-80502885-G-C
• gnomAD v3: 5-81207066-G-C
• gnomAD v4: 5-81207066-G-C
• MyVariant Identifiers: chr5:g.80502885G>C (hg19) ; chr5:g.81207066G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81207066G>C , CM000667.2:g.81207066G>C	GRCh38
NC_000005.9:g.80502885G>C , CM000667.1:g.80502885G>C	GRCh37
NC_000005.8:g.80538641G>C	NCBI36
NG_030334.1:g.251378G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265080.9:c.2967+161G>C MANE Select	ENSP00000265080.4:n.2967+161G>C
ENST00000265080.8:c.2967+161G>C	ENSP00000265080.4:n.2967+161G>C
ENST00000503795.1:c.2967+161G>C	ENSP00000421771.1:n.2967+161G>C
NM_006909.2:c.2967+161G>C	NP_008840.1:n.2967+161G>C
XM_017009682.2:c.2682+161G>C	XP_016865171.1:n.2682+161G>C
XR_002956166.1:n.3083+161G>C
NM_006909.3:c.2967+161G>C MANE Select	NP_008840.1:n.2967+161G>C