Canonical Allele Identifier: CA2651759272
Gene: MAVS HGNC NCBI

Linked Data

gnomAD v4: 20-3857873-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857873C>A , CM000682.2:g.3857873C>A GRCh38
NC_000020.10:g.3838520C>A , CM000682.1:g.3838520C>A GRCh37
NC_000020.9:g.3786520C>A NCBI36
NG_030028.1:g.16075C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.292+64C>A MANE Select ENSP00000401980.2:n.292+64C>A
ENST00000416600.6:c.-132+3132C>A ENSP00000413749.2:n.-132+3132C>A
ENST00000428216.3:c.292+64C>A ENSP00000401980.2:n.292+64C>A
NM_001206491.1:c.-132+3132C>A NP_001193420.1:n.-132+3132C>A
NM_020746.4:c.292+64C>A NP_065797.2:n.292+64C>A
NR_037921.1:n.464+64C>A
NM_020746.5:c.292+64C>A MANE Select NP_065797.2:n.292+64C>A
NR_037921.2:n.429+64C>A
NM_001206491.2:c.-132+3132C>A NP_001193420.1:n.-132+3132C>A
NM_001385663.1:c.-256+64C>A NP_001372592.1:n.-256+64C>A