Canonical Allele Identifier: CA408119031
Gene: MAVS HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.3838378T>A (hg19) chr20:g.3857731T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857731T>A , CM000682.2:g.3857731T>A GRCh38
NC_000020.10:g.3838378T>A , CM000682.1:g.3838378T>A GRCh37
NC_000020.9:g.3786378T>A NCBI36
NG_030028.1:g.15933T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.214T>A MANE Select ENSP00000401980.2:p.Phe72Ile
ENST00000416600.6:c.-132+2990T>A ENSP00000413749.2:n.-132+2990T>A
ENST00000428216.3:c.214T>A ENSP00000401980.2:p.Phe72Ile
NM_001206491.1:c.-132+2990T>A NP_001193420.1:n.-132+2990T>A
NM_020746.4:c.214T>A NP_065797.2:p.Phe72Ile
NR_037921.1:n.386T>A
NM_020746.5:c.214T>A MANE Select NP_065797.2:p.Phe72Ile
NR_037921.2:n.351T>A
NM_001206491.2:c.-132+2990T>A NP_001193420.1:n.-132+2990T>A
NM_001385663.1:c.-334T>A NP_001372592.1:n.-334T>A
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