Canonical Allele Identifier: CA814488184

Gene: RASGRF2

Linked Data

• dbSNP Id: rs1421626463
• MyVariant Identifiers: chr5:g.80502555del (hg19) ; chr5:g.81206736del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81206736del , CM000667.2:g.81206736del	GRCh38
NC_000005.9:g.80502555del , CM000667.1:g.80502555del	GRCh37
NC_000005.8:g.80538311del	NCBI36
NG_030334.1:g.251048del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265080.9:c.2907-109del MANE Select	ENSP00000265080.4:n.2907-109del
ENST00000265080.8:c.2907-109del	ENSP00000265080.4:n.2907-109del
ENST00000503795.1:c.2907-109del	ENSP00000421771.1:n.2907-109del
NM_006909.2:c.2907-109del	NP_008840.1:n.2907-109del
XM_017009682.2:c.2622-109del	XP_016865171.1:n.2622-109del
XR_002956166.1:n.3023-109del
NM_006909.3:c.2907-109del MANE Select	NP_008840.1:n.2907-109del