Canonical Allele Identifier: CA814488519

Gene: RASGRF2

Linked Data

• dbSNP Id: rs1193699101
• gnomAD v3: 5-81207085-G-T
• gnomAD v4: 5-81207085-G-T
• MyVariant Identifiers: chr5:g.80502904G>T (hg19) ; chr5:g.81207085G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.81207085G>T , CM000667.2:g.81207085G>T	GRCh38
NC_000005.9:g.80502904G>T , CM000667.1:g.80502904G>T	GRCh37
NC_000005.8:g.80538660G>T	NCBI36
NG_030334.1:g.251397G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265080.9:c.2968-161G>T MANE Select	ENSP00000265080.4:n.2968-161G>T
ENST00000265080.8:c.2968-161G>T	ENSP00000265080.4:n.2968-161G>T
ENST00000503795.1:c.2968-161G>T	ENSP00000421771.1:n.2968-161G>T
NM_006909.2:c.2968-161G>T	NP_008840.1:n.2968-161G>T
XM_017009682.2:c.2683-161G>T	XP_016865171.1:n.2683-161G>T
XR_002956166.1:n.3084-161G>T
NM_006909.3:c.2968-161G>T MANE Select	NP_008840.1:n.2968-161G>T