Canonical Allele Identifier: CA531774034

Gene: RASGRP3

Linked Data

• dbSNP Id: rs1215080116
• gnomAD v2: 2-33682778-T-C
• gnomAD v3: 2-33457711-T-C
• gnomAD v4: 2-33457711-T-C
• MyVariant Identifiers: chr2:g.33682778T>C (hg19) ; chr2:g.33457711T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33457711T>C , CM000664.2:g.33457711T>C	GRCh38
NC_000002.11:g.33682778T>C , CM000664.1:g.33682778T>C	GRCh37
NC_000002.10:g.33536282T>C	NCBI36
NG_053077.1:g.26364T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+9768T>C	ENSP00000385886.3:n.-261+9768T>C
ENST00000479528.5:n.149+9768T>C
ENST00000484909.5:n.390+9768T>C
ENST00000497723.6:n.303+9768T>C
NM_170672.2:c.-261+9768T>C	NP_733772.1:n.-261+9768T>C
XM_011532746.1:c.-159+9768T>C	XP_011531048.1:n.-159+9768T>C
NM_001349975.1:c.-383+9768T>C	NP_001336904.1:n.-383+9768T>C
NM_001349978.1:c.-261+9768T>C	NP_001336907.1:n.-261+9768T>C
XM_011532746.3:c.-159+9768T>C	XP_011531048.1:n.-159+9768T>C
XM_017003759.2:c.-1635+9768T>C	XP_016859248.1:n.-1635+9768T>C
NM_001349975.2:c.-383+9768T>C	NP_001336904.1:n.-383+9768T>C
NM_001349978.2:c.-261+9768T>C	NP_001336907.1:n.-261+9768T>C
NM_170672.3:c.-261+9768T>C	NP_733772.1:n.-261+9768T>C