Canonical Allele Identifier: CA10581500
Gene: RASGRP3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 236028
ClinVar RCV Id: RCV000225002
dbSNP Id: rs2124437

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.33457670G>T , CM000664.2:g.33457670G>T GRCh38
NC_000002.10:g.33536241G>T NCBI36
NC_000002.11:g.33682737G>T , CM000664.1:g.33682737G>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000402538.7:c.-261+9727G>T ENSP00000385886.3:p.=
ENST00000479528.5:n.149+9727G>T
ENST00000484909.5:n.390+9727G>T
ENST00000497723.6:n.303+9727G>T
NM_170672.2:c.-261+9727G>T VV NP_733772.1:p.=
XM_011532746.1:c.-159+9727G>T XP_011531048.1:p.=