Canonical Allele Identifier: CA767954054

Gene: RASGRP3

Linked Data

• dbSNP Id: rs1331797444
• MyVariant Identifiers: chr2:g.33682718A>T (hg19) ; chr2:g.33457651A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33457651A>T , CM000664.2:g.33457651A>T	GRCh38
NC_000002.11:g.33682718A>T , CM000664.1:g.33682718A>T	GRCh37
NC_000002.10:g.33536222A>T	NCBI36
NG_053077.1:g.26304A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+9708A>T	ENSP00000385886.3:n.-261+9708A>T
ENST00000479528.5:n.149+9708A>T
ENST00000484909.5:n.390+9708A>T
ENST00000497723.6:n.303+9708A>T
NM_170672.2:c.-261+9708A>T	NP_733772.1:n.-261+9708A>T
XM_011532746.1:c.-159+9708A>T	XP_011531048.1:n.-159+9708A>T
NM_001349975.1:c.-383+9708A>T	NP_001336904.1:n.-383+9708A>T
NM_001349978.1:c.-261+9708A>T	NP_001336907.1:n.-261+9708A>T
XM_011532746.3:c.-159+9708A>T	XP_011531048.1:n.-159+9708A>T
XM_017003759.2:c.-1635+9708A>T	XP_016859248.1:n.-1635+9708A>T
NM_001349975.2:c.-383+9708A>T	NP_001336904.1:n.-383+9708A>T
NM_001349978.2:c.-261+9708A>T	NP_001336907.1:n.-261+9708A>T
NM_170672.3:c.-261+9708A>T	NP_733772.1:n.-261+9708A>T