Canonical Allele Identifier: CA2346769771
Gene: MAVS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857858C= , CM000682.2:g.3857858C= GRCh38
NC_000020.10:g.3838505C= , CM000682.1:g.3838505C= GRCh37
NC_000020.9:g.3786505C= NCBI36
NG_030028.1:g.16060C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.292+49C= MANE Select ENSP00000401980.2:n.292+49C=
ENST00000416600.6:c.-132+3117C= ENSP00000413749.2:n.-132+3117C=
ENST00000428216.3:c.292+49C= ENSP00000401980.2:n.292+49C=
NM_001206491.1:c.-132+3117C= NP_001193420.1:n.-132+3117C=
NM_020746.4:c.292+49C= NP_065797.2:n.292+49C=
NR_037921.1:n.464+49C=
NM_020746.5:c.292+49C= MANE Select NP_065797.2:n.292+49C=
NR_037921.2:n.429+49C=
NM_001206491.2:c.-132+3117C= NP_001193420.1:n.-132+3117C=
NM_001385663.1:c.-256+49C= NP_001372592.1:n.-256+49C=
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