Canonical Allele Identifier: CA72138822

Gene: RBMS3

Linked Data

• dbSNP Id: rs957409374
• MyVariant Identifiers: chr3:g.29954628C>T (hg19) ; chr3:g.29913137C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.29913137C>T , CM000665.2:g.29913137C>T	GRCh38
NC_000003.11:g.29954628C>T , CM000665.1:g.29954628C>T	GRCh37
NC_000003.10:g.29929632C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000383767.7:c.939+13382C>T MANE Select	ENSP00000373277.2:n.939+13382C>T
ENST00000636680.2:c.1317+13382C>T	ENSP00000490271.2:n.1317+13382C>T
ENST00000637842.1:c.1186+13382C>T	ENSP00000489718.1:n.1186+13382C>T
ENST00000273139.13:c.939+13382C>T	ENSP00000273139.9:n.939+13382C>T
ENST00000383766.6:c.885+15662C>T	ENSP00000373276.2:n.885+15662C>T
ENST00000383767.6:c.939+13382C>T	ENSP00000373277.2:n.939+13382C>T
ENST00000434693.6:c.936+13382C>T	ENSP00000395592.1:n.936+13382C>T
ENST00000452462.5:c.939+13382C>T	ENSP00000397926.1:n.939+13382C>T
ENST00000456853.1:c.978+13382C>T	ENSP00000400519.1:n.978+13382C>T
NM_001003792.2:c.885+15662C>T	NP_001003792.1:n.885+15662C>T
NM_001003793.2:c.939+13382C>T	NP_001003793.1:n.939+13382C>T
NM_001177711.1:c.939+13382C>T	NP_001171182.1:n.939+13382C>T
NM_001177712.1:c.978+13382C>T	NP_001171183.1:n.978+13382C>T
NM_014483.3:c.939+13382C>T	NP_055298.2:n.939+13382C>T
XM_005265060.1:c.936+13382C>T	XP_005265117.1:n.936+13382C>T
XM_005265061.1:c.888+15662C>T	XP_005265118.1:n.888+15662C>T
XM_005265062.1:c.888+15662C>T	XP_005265119.1:n.888+15662C>T
XM_005265063.1:c.654+13382C>T	XP_005265120.1:n.654+13382C>T
XM_005265064.3:c.654+13382C>T	XP_005265121.1:n.654+13382C>T
XM_005265065.3:c.612+13382C>T	XP_005265122.1:n.612+13382C>T
XM_011533592.1:c.939+13382C>T	XP_011531894.1:n.939+13382C>T
XM_011533593.1:c.939+13382C>T	XP_011531895.1:n.939+13382C>T
XM_011533594.1:c.940-11160C>T	XP_011531896.1:n.940-11160C>T
NM_001330696.1:c.936+13382C>T	NP_001317625.1:n.936+13382C>T
XM_005265061.2:c.888+15662C>T	XP_005265118.1:n.888+15662C>T
XM_005265063.2:c.654+13382C>T	XP_005265120.1:n.654+13382C>T
XM_005265065.5:c.612+13382C>T	XP_005265122.1:n.612+13382C>T
XM_017006178.1:c.936+13382C>T	XP_016861667.1:n.936+13382C>T
XM_017006179.1:c.936+13382C>T	XP_016861668.1:n.936+13382C>T
XM_017006180.1:c.888+15662C>T	XP_016861669.1:n.888+15662C>T
XM_017006181.1:c.885+15662C>T	XP_016861670.1:n.885+15662C>T
XM_017006182.1:c.786+15662C>T	XP_016861671.1:n.786+15662C>T
XM_024453454.1:c.939+13382C>T	XP_024309222.1:n.939+13382C>T
NM_001003792.3:c.885+15662C>T	NP_001003792.1:n.885+15662C>T
NM_001003793.3:c.939+13382C>T MANE Select	NP_001003793.1:n.939+13382C>T
NM_001177711.2:c.939+13382C>T	NP_001171182.1:n.939+13382C>T
NM_001177712.2:c.978+13382C>T	NP_001171183.1:n.978+13382C>T
NM_014483.4:c.939+13382C>T	NP_055298.2:n.939+13382C>T