Canonical Allele Identifier: CA1029131558

Gene: RASGRP3

Linked Data

• gnomAD v3: 2-33457572-C-T
• gnomAD v4: 2-33457572-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33457572C>T , CM000664.2:g.33457572C>T	GRCh38
NC_000002.11:g.33682639C>T , CM000664.1:g.33682639C>T	GRCh37
NC_000002.10:g.33536143C>T	NCBI36
NG_053077.1:g.26225C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000402538.7:c.-261+9629C>T	ENSP00000385886.3:n.-261+9629C>T
ENST00000479528.5:n.149+9629C>T
ENST00000484909.5:n.390+9629C>T
ENST00000497723.6:n.303+9629C>T
NM_170672.2:c.-261+9629C>T	NP_733772.1:n.-261+9629C>T
XM_011532746.1:c.-159+9629C>T	XP_011531048.1:n.-159+9629C>T
NM_001349975.1:c.-383+9629C>T	NP_001336904.1:n.-383+9629C>T
NM_001349978.1:c.-261+9629C>T	NP_001336907.1:n.-261+9629C>T
XM_011532746.3:c.-159+9629C>T	XP_011531048.1:n.-159+9629C>T
XM_017003759.2:c.-1635+9629C>T	XP_016859248.1:n.-1635+9629C>T
NM_001349975.2:c.-383+9629C>T	NP_001336904.1:n.-383+9629C>T
NM_001349978.2:c.-261+9629C>T	NP_001336907.1:n.-261+9629C>T
NM_170672.3:c.-261+9629C>T	NP_733772.1:n.-261+9629C>T