Canonical Allele Identifier: CA814488247

Gene: RASGRF2

Linked Data

• dbSNP Id: rs1284418843
• MyVariant Identifiers: chr5:g.80502645A>T (hg19) ; chr5:g.81206826A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81206826A>T , CM000667.2:g.81206826A>T	GRCh38
NC_000005.9:g.80502645A>T , CM000667.1:g.80502645A>T	GRCh37
NC_000005.8:g.80538401A>T	NCBI36
NG_030334.1:g.251138A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265080.9:c.2907-19A>T MANE Select	ENSP00000265080.4:n.2907-19A>T
ENST00000265080.8:c.2907-19A>T	ENSP00000265080.4:n.2907-19A>T
ENST00000503795.1:c.2907-19A>T	ENSP00000421771.1:n.2907-19A>T
NM_006909.2:c.2907-19A>T	NP_008840.1:n.2907-19A>T
XM_017009682.2:c.2622-19A>T	XP_016865171.1:n.2622-19A>T
XR_002956166.1:n.3023-19A>T
NM_006909.3:c.2907-19A>T MANE Select	NP_008840.1:n.2907-19A>T