Canonical Allele Identifier: CA408119156
Gene: MAVS HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.3838435G>C (hg19) chr20:g.3857788G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857788G>C , CM000682.2:g.3857788G>C GRCh38
NC_000020.10:g.3838435G>C , CM000682.1:g.3838435G>C GRCh37
NC_000020.9:g.3786435G>C NCBI36
NG_030028.1:g.15990G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.271G>C MANE Select ENSP00000401980.2:p.Val91Leu
ENST00000416600.6:c.-132+3047G>C ENSP00000413749.2:n.-132+3047G>C
ENST00000428216.3:c.271G>C ENSP00000401980.2:p.Val91Leu
NM_001206491.1:c.-132+3047G>C NP_001193420.1:n.-132+3047G>C
NM_020746.4:c.271G>C NP_065797.2:p.Val91Leu
NR_037921.1:n.443G>C
NM_020746.5:c.271G>C MANE Select NP_065797.2:p.Val91Leu
NR_037921.2:n.408G>C
NM_001206491.2:c.-132+3047G>C NP_001193420.1:n.-132+3047G>C
NM_001385663.1:c.-277G>C NP_001372592.1:n.-277G>C
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