Canonical Allele Identifier: CA1078013968

Gene: RASGRF2

Linked Data

• dbSNP Id: rs1755526416
• gnomAD v3: 5-81207164-C-CAGCT
• gnomAD v4: 5-81207164-C-CAGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81207165_81207168dup , CM000667.2:g.81207165_81207168dup	GRCh38
NC_000005.9:g.80502984_80502987dup , CM000667.1:g.80502984_80502987dup	GRCh37
NC_000005.8:g.80538740_80538743dup	NCBI36
NG_030334.1:g.251477_251480dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265080.9:c.2968-81_2968-78dup MANE Select	ENSP00000265080.4:n.2968-81_2968-78dup
ENST00000265080.8:c.2968-81_2968-78dup	ENSP00000265080.4:n.2968-81_2968-78dup
ENST00000503795.1:c.2968-81_2968-78dup	ENSP00000421771.1:n.2968-81_2968-78dup
NM_006909.2:c.2968-81_2968-78dup	NP_008840.1:n.2968-81_2968-78dup
XM_017009682.2:c.2683-81_2683-78dup	XP_016865171.1:n.2683-81_2683-78dup
XR_002956166.1:n.3084-81_3084-78dup
NM_006909.3:c.2968-81_2968-78dup MANE Select	NP_008840.1:n.2968-81_2968-78dup