Canonical Allele Identifier: CA2736356227

Gene: MAVS

Linked Data

• dbSNP Id: rs2146765629

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857847T>G , CM000682.2:g.3857847T>G	GRCh38
NC_000020.10:g.3838494T>G , CM000682.1:g.3838494T>G	GRCh37
NC_000020.9:g.3786494T>G	NCBI36
NG_030028.1:g.16049T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.292+38T>G MANE Select	ENSP00000401980.2:n.292+38T>G
ENST00000416600.6:c.-132+3106T>G	ENSP00000413749.2:n.-132+3106T>G
ENST00000428216.3:c.292+38T>G	ENSP00000401980.2:n.292+38T>G
NM_001206491.1:c.-132+3106T>G	NP_001193420.1:n.-132+3106T>G
NM_020746.4:c.292+38T>G	NP_065797.2:n.292+38T>G
NR_037921.1:n.464+38T>G
NM_020746.5:c.292+38T>G MANE Select	NP_065797.2:n.292+38T>G
NR_037921.2:n.429+38T>G
NM_001206491.2:c.-132+3106T>G	NP_001193420.1:n.-132+3106T>G
NM_001385663.1:c.-256+38T>G	NP_001372592.1:n.-256+38T>G