Canonical Allele Identifier: CA1078013959
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs1377785753
gnomAD v3: 5-81207114-AT-A
gnomAD v4: 5-81207114-AT-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207121del , CM000667.2:g.81207121del GRCh38
NC_000005.9:g.80502940del , CM000667.1:g.80502940del GRCh37
NC_000005.8:g.80538696del NCBI36
NG_030334.1:g.251433del

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.2968-125del MANE Select ENSP00000265080.4:n.2968-125del
ENST00000265080.8:c.2968-125del ENSP00000265080.4:n.2968-125del
ENST00000503795.1:c.2968-125del ENSP00000421771.1:n.2968-125del
NM_006909.2:c.2968-125del NP_008840.1:n.2968-125del
XM_017009682.2:c.2683-125del XP_016865171.1:n.2683-125del
XR_002956166.1:n.3084-125del
NM_006909.3:c.2968-125del MANE Select NP_008840.1:n.2968-125del
Search 100 bp 5'
Search 100 bp 3'