Canonical Allele Identifier: CA44891892

Gene: RASGRP3

Linked Data

• dbSNP Id: rs368054200
• gnomAD v2: 2-33682758-C-G
• gnomAD v3: 2-33457691-C-G
• gnomAD v4: 2-33457691-C-G
• MyVariant Identifiers: chr2:g.33682758C>G (hg19) ; chr2:g.33457691C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33457691C>G , CM000664.2:g.33457691C>G	GRCh38
NC_000002.11:g.33682758C>G , CM000664.1:g.33682758C>G	GRCh37
NC_000002.10:g.33536262C>G	NCBI36
NG_053077.1:g.26344C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+9748C>G	ENSP00000385886.3:n.-261+9748C>G
ENST00000479528.5:n.149+9748C>G
ENST00000484909.5:n.390+9748C>G
ENST00000497723.6:n.303+9748C>G
NM_170672.2:c.-261+9748C>G	NP_733772.1:n.-261+9748C>G
XM_011532746.1:c.-159+9748C>G	XP_011531048.1:n.-159+9748C>G
NM_001349975.1:c.-383+9748C>G	NP_001336904.1:n.-383+9748C>G
NM_001349978.1:c.-261+9748C>G	NP_001336907.1:n.-261+9748C>G
XM_011532746.3:c.-159+9748C>G	XP_011531048.1:n.-159+9748C>G
XM_017003759.2:c.-1635+9748C>G	XP_016859248.1:n.-1635+9748C>G
NM_001349975.2:c.-383+9748C>G	NP_001336904.1:n.-383+9748C>G
NM_001349978.2:c.-261+9748C>G	NP_001336907.1:n.-261+9748C>G
NM_170672.3:c.-261+9748C>G	NP_733772.1:n.-261+9748C>G