Canonical Allele Identifier: CA408119162
Gene: MAVS HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.3838438T>A (hg19) chr20:g.3857791T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857791T>A , CM000682.2:g.3857791T>A GRCh38
NC_000020.10:g.3838438T>A , CM000682.1:g.3838438T>A GRCh37
NC_000020.9:g.3786438T>A NCBI36
NG_030028.1:g.15993T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.274T>A MANE Select ENSP00000401980.2:p.Tyr92Asn
ENST00000416600.6:c.-132+3050T>A ENSP00000413749.2:n.-132+3050T>A
ENST00000428216.3:c.274T>A ENSP00000401980.2:p.Tyr92Asn
NM_001206491.1:c.-132+3050T>A NP_001193420.1:n.-132+3050T>A
NM_020746.4:c.274T>A NP_065797.2:p.Tyr92Asn
NR_037921.1:n.446T>A
NM_020746.5:c.274T>A MANE Select NP_065797.2:p.Tyr92Asn
NR_037921.2:n.411T>A
NM_001206491.2:c.-132+3050T>A NP_001193420.1:n.-132+3050T>A
NM_001385663.1:c.-274T>A NP_001372592.1:n.-274T>A
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