Canonical Allele Identifier: CA408119104
Gene: MAVS HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.3838409T>A (hg19) chr20:g.3857762T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857762T>A , CM000682.2:g.3857762T>A GRCh38
NC_000020.10:g.3838409T>A , CM000682.1:g.3838409T>A GRCh37
NC_000020.9:g.3786409T>A NCBI36
NG_030028.1:g.15964T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.245T>A MANE Select ENSP00000401980.2:p.Val82Asp
ENST00000416600.6:c.-132+3021T>A ENSP00000413749.2:n.-132+3021T>A
ENST00000428216.3:c.245T>A ENSP00000401980.2:p.Val82Asp
NM_001206491.1:c.-132+3021T>A NP_001193420.1:n.-132+3021T>A
NM_020746.4:c.245T>A NP_065797.2:p.Val82Asp
NR_037921.1:n.417T>A
NM_020746.5:c.245T>A MANE Select NP_065797.2:p.Val82Asp
NR_037921.2:n.382T>A
NM_001206491.2:c.-132+3021T>A NP_001193420.1:n.-132+3021T>A
NM_001385663.1:c.-303T>A NP_001372592.1:n.-303T>A
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