Canonical Allele Identifier: CA2346769643
Gene: MAVS HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857612G= , CM000682.2:g.3857612G= GRCh38
NC_000020.10:g.3838259G= , CM000682.1:g.3838259G= GRCh37
NC_000020.9:g.3786259G= NCBI36
NG_030028.1:g.15814G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.118-23G= MANE Select ENSP00000401980.2:n.118-23G=
ENST00000416600.6:c.-132+2871G= ENSP00000413749.2:n.-132+2871G=
ENST00000428216.3:c.118-23G= ENSP00000401980.2:n.118-23G=
NM_001206491.1:c.-132+2871G= NP_001193420.1:n.-132+2871G=
NM_020746.4:c.118-23G= NP_065797.2:n.118-23G=
NR_037921.1:n.290-23G=
NM_020746.5:c.118-23G= MANE Select NP_065797.2:n.118-23G=
NR_037921.2:n.255-23G=
NM_001206491.2:c.-132+2871G= NP_001193420.1:n.-132+2871G=
NM_001385663.1:c.-430-23G= NP_001372592.1:n.-430-23G=
Search 100 bp 5'
Search 100 bp 3'