Canonical Allele Identifier: CA2346769775
Gene: MAVS HGNC NCBI

Linked Data

dbSNP Id: rs2089826109

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857865C>G , CM000682.2:g.3857865C>G GRCh38
NC_000020.10:g.3838512C>G , CM000682.1:g.3838512C>G GRCh37
NC_000020.9:g.3786512C>G NCBI36
NG_030028.1:g.16067C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.292+56C>G MANE Select ENSP00000401980.2:n.292+56C>G
ENST00000416600.6:c.-132+3124C>G ENSP00000413749.2:n.-132+3124C>G
ENST00000428216.3:c.292+56C>G ENSP00000401980.2:n.292+56C>G
NM_001206491.1:c.-132+3124C>G NP_001193420.1:n.-132+3124C>G
NM_020746.4:c.292+56C>G NP_065797.2:n.292+56C>G
NR_037921.1:n.464+56C>G
NM_020746.5:c.292+56C>G MANE Select NP_065797.2:n.292+56C>G
NR_037921.2:n.429+56C>G
NM_001206491.2:c.-132+3124C>G NP_001193420.1:n.-132+3124C>G
NM_001385663.1:c.-256+56C>G NP_001372592.1:n.-256+56C>G