Canonical Allele Identifier: CA44892195

Gene: RASGRP3

Linked Data

• dbSNP Id: rs1035736469
• gnomAD v3: 2-33458028-G-A
• gnomAD v4: 2-33458028-G-A
• MyVariant Identifiers: chr2:g.33683095G>A (hg19) ; chr2:g.33458028G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33458028G>A , CM000664.2:g.33458028G>A	GRCh38
NC_000002.11:g.33683095G>A , CM000664.1:g.33683095G>A	GRCh37
NC_000002.10:g.33536599G>A	NCBI36
NG_053077.1:g.26681G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+10085G>A	ENSP00000385886.3:n.-261+10085G>A
ENST00000479528.5:n.149+10085G>A
ENST00000484909.5:n.390+10085G>A
ENST00000497723.6:n.303+10085G>A
NM_170672.2:c.-261+10085G>A	NP_733772.1:n.-261+10085G>A
XM_011532746.1:c.-159+10085G>A	XP_011531048.1:n.-159+10085G>A
NM_001349975.1:c.-383+10085G>A	NP_001336904.1:n.-383+10085G>A
NM_001349978.1:c.-261+10085G>A	NP_001336907.1:n.-261+10085G>A
XM_011532746.3:c.-159+10085G>A	XP_011531048.1:n.-159+10085G>A
XM_017003759.2:c.-1635+10085G>A	XP_016859248.1:n.-1635+10085G>A
NM_001349975.2:c.-383+10085G>A	NP_001336904.1:n.-383+10085G>A
NM_001349978.2:c.-261+10085G>A	NP_001336907.1:n.-261+10085G>A
NM_170672.3:c.-261+10085G>A	NP_733772.1:n.-261+10085G>A