Canonical Allele Identifier: CA531774031

Gene: RASGRP3

Linked Data

• dbSNP Id: rs1274429525
• gnomAD v2: 2-33682701-C-T
• gnomAD v3: 2-33457634-C-T
• gnomAD v4: 2-33457634-C-T
• MyVariant Identifiers: chr2:g.33682701C>T (hg19) ; chr2:g.33457634C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33457634C>T , CM000664.2:g.33457634C>T	GRCh38
NC_000002.11:g.33682701C>T , CM000664.1:g.33682701C>T	GRCh37
NC_000002.10:g.33536205C>T	NCBI36
NG_053077.1:g.26287C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+9691C>T	ENSP00000385886.3:n.-261+9691C>T
ENST00000479528.5:n.149+9691C>T
ENST00000484909.5:n.390+9691C>T
ENST00000497723.6:n.303+9691C>T
NM_170672.2:c.-261+9691C>T	NP_733772.1:n.-261+9691C>T
XM_011532746.1:c.-159+9691C>T	XP_011531048.1:n.-159+9691C>T
NM_001349975.1:c.-383+9691C>T	NP_001336904.1:n.-383+9691C>T
NM_001349978.1:c.-261+9691C>T	NP_001336907.1:n.-261+9691C>T
XM_011532746.3:c.-159+9691C>T	XP_011531048.1:n.-159+9691C>T
XM_017003759.2:c.-1635+9691C>T	XP_016859248.1:n.-1635+9691C>T
NM_001349975.2:c.-383+9691C>T	NP_001336904.1:n.-383+9691C>T
NM_001349978.2:c.-261+9691C>T	NP_001336907.1:n.-261+9691C>T
NM_170672.3:c.-261+9691C>T	NP_733772.1:n.-261+9691C>T