Canonical Allele Identifier: CA509425226
Gene: MAVS HGNC NCBI

Linked Data

gnomAD v4: 20-3857661-C-T
MyVariant Identifiers: chr20:g.3838308C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857661C>T , CM000682.2:g.3857661C>T GRCh38
NC_000020.10:g.3838308C>T , CM000682.1:g.3838308C>T GRCh37
NC_000020.9:g.3786308C>T NCBI36
NG_030028.1:g.15863C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.144C>T MANE Select ENSP00000401980.2:p.Leu48=
ENST00000416600.6:c.-132+2920C>T ENSP00000413749.2:n.-132+2920C>T
ENST00000428216.3:c.144C>T ENSP00000401980.2:p.Leu48=
NM_001206491.1:c.-132+2920C>T NP_001193420.1:n.-132+2920C>T
NM_020746.4:c.144C>T NP_065797.2:p.Leu48=
NR_037921.1:n.316C>T
NM_020746.5:c.144C>T MANE Select NP_065797.2:p.Leu48=
NR_037921.2:n.281C>T
NM_001206491.2:c.-132+2920C>T NP_001193420.1:n.-132+2920C>T
NM_001385663.1:c.-404C>T NP_001372592.1:n.-404C>T