Canonical Allele Identifier: CA360289507
Gene: RASGRF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.80502663G>A (hg19) chr5:g.81206844G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206844G>A , CM000667.2:g.81206844G>A GRCh38
NC_000005.9:g.80502663G>A , CM000667.1:g.80502663G>A GRCh37
NC_000005.8:g.80538419G>A NCBI36
NG_030334.1:g.251156G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2907-1G>A MANE Select ENSP00000265080.4:n.2907-1G>A
ENST00000265080.8:c.2907-1G>A ENSP00000265080.4:n.2907-1G>A
ENST00000503795.1:c.2907-1G>A ENSP00000421771.1:n.2907-1G>A
NM_006909.2:c.2907-1G>A NP_008840.1:n.2907-1G>A
XM_017009682.2:c.2622-1G>A XP_016865171.1:n.2622-1G>A
XR_002956166.1:n.3023-1G>A
NM_006909.3:c.2907-1G>A MANE Select NP_008840.1:n.2907-1G>A
Search 100 bp 5'
Search 100 bp 3'