Canonical Allele Identifier: CA509425320
Gene: MAVS HGNC NCBI

Linked Data

dbSNP Id: rs1402528415
gnomAD v2: 20-3838407-A-G
gnomAD v4: 20-3857760-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857760A>G , CM000682.2:g.3857760A>G GRCh38
NC_000020.10:g.3838407A>G , CM000682.1:g.3838407A>G GRCh37
NC_000020.9:g.3786407A>G NCBI36
NG_030028.1:g.15962A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.243A>G MANE Select ENSP00000401980.2:p.Leu81=
ENST00000416600.6:c.-132+3019A>G ENSP00000413749.2:n.-132+3019A>G
ENST00000428216.3:c.243A>G ENSP00000401980.2:p.Leu81=
NM_001206491.1:c.-132+3019A>G NP_001193420.1:n.-132+3019A>G
NM_020746.4:c.243A>G NP_065797.2:p.Leu81=
NR_037921.1:n.415A>G
NM_020746.5:c.243A>G MANE Select NP_065797.2:p.Leu81=
NR_037921.2:n.380A>G
NM_001206491.2:c.-132+3019A>G NP_001193420.1:n.-132+3019A>G
NM_001385663.1:c.-305A>G NP_001372592.1:n.-305A>G