Canonical Allele Identifier: CA408118533
Gene: MAVS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857666G>T , CM000682.2:g.3857666G>T GRCh38
NC_000020.10:g.3838313G>T , CM000682.1:g.3838313G>T GRCh37
NC_000020.9:g.3786313G>T NCBI36
NG_030028.1:g.15868G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.149G>T MANE Select ENSP00000401980.2:p.Gly50Val
ENST00000416600.6:c.-132+2925G>T ENSP00000413749.2:n.-132+2925G>T
ENST00000428216.3:c.149G>T ENSP00000401980.2:p.Gly50Val
NM_001206491.1:c.-132+2925G>T NP_001193420.1:n.-132+2925G>T
NM_020746.4:c.149G>T NP_065797.2:p.Gly50Val
NR_037921.1:n.321G>T
NM_020746.5:c.149G>T MANE Select NP_065797.2:p.Gly50Val
NR_037921.2:n.286G>T
NM_001206491.2:c.-132+2925G>T NP_001193420.1:n.-132+2925G>T
NM_001385663.1:c.-399G>T NP_001372592.1:n.-399G>T