Canonical Allele Identifier: CA9750009
Gene: MAVS HGNC NCBI

Linked Data

dbSNP Id: rs745383241
gnomAD v2: 20-3838421-A-G
gnomAD v4: 20-3857774-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857774A>G , CM000682.2:g.3857774A>G GRCh38
NC_000020.10:g.3838421A>G , CM000682.1:g.3838421A>G GRCh37
NC_000020.9:g.3786421A>G NCBI36
NG_030028.1:g.15976A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.257A>G MANE Select ENSP00000401980.2:p.Asp86Gly
ENST00000416600.6:c.-132+3033A>G ENSP00000413749.2:n.-132+3033A>G
ENST00000428216.3:c.257A>G ENSP00000401980.2:p.Asp86Gly
NM_001206491.1:c.-132+3033A>G NP_001193420.1:n.-132+3033A>G
NM_020746.4:c.257A>G NP_065797.2:p.Asp86Gly
NR_037921.1:n.429A>G
NM_020746.5:c.257A>G MANE Select NP_065797.2:p.Asp86Gly
NR_037921.2:n.394A>G
NM_001206491.2:c.-132+3033A>G NP_001193420.1:n.-132+3033A>G
NM_001385663.1:c.-291A>G NP_001372592.1:n.-291A>G