Canonical Allele Identifier: CA1243165090

Gene: RASGRP3

Linked Data

• dbSNP Id: rs1666140012

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33458057C>G , CM000664.2:g.33458057C>G	GRCh38
NC_000002.11:g.33683124C>G , CM000664.1:g.33683124C>G	GRCh37
NC_000002.10:g.33536628C>G	NCBI36
NG_053077.1:g.26710C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+10114C>G	ENSP00000385886.3:n.-261+10114C>G
ENST00000437184.5:c.-334C>G	ENSP00000393866.1:n.-334C>G
ENST00000479528.5:n.149+10114C>G
ENST00000484909.5:n.390+10114C>G
ENST00000497723.6:n.303+10114C>G
NM_170672.2:c.-261+10114C>G	NP_733772.1:n.-261+10114C>G
XM_011532746.1:c.-159+10114C>G	XP_011531048.1:n.-159+10114C>G
NM_001349975.1:c.-383+10114C>G	NP_001336904.1:n.-383+10114C>G
NM_001349978.1:c.-261+10114C>G	NP_001336907.1:n.-261+10114C>G
NM_001349979.1:c.-334C>G	NP_001336908.1:n.-334C>G
XM_011532746.3:c.-159+10114C>G	XP_011531048.1:n.-159+10114C>G
XM_011532748.3:c.-334C>G	XP_011531050.2:n.-334C>G
XM_017003759.2:c.-1635+10114C>G	XP_016859248.1:n.-1635+10114C>G
NM_001349975.2:c.-383+10114C>G	NP_001336904.1:n.-383+10114C>G
NM_001349978.2:c.-261+10114C>G	NP_001336907.1:n.-261+10114C>G
NM_001349979.2:c.-334C>G	NP_001336908.1:n.-334C>G
NM_170672.3:c.-261+10114C>G	NP_733772.1:n.-261+10114C>G