Canonical Allele Identifier: CA2346769623
Gene: MAVS HGNC NCBI

Linked Data

dbSNP Id: rs1600447814

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857559G>T , CM000682.2:g.3857559G>T GRCh38
NC_000020.10:g.3838206G>T , CM000682.1:g.3838206G>T GRCh37
NC_000020.9:g.3786206G>T NCBI36
NG_030028.1:g.15761G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.118-76G>T MANE Select ENSP00000401980.2:n.118-76G>T
ENST00000416600.6:c.-132+2818G>T ENSP00000413749.2:n.-132+2818G>T
ENST00000428216.3:c.118-76G>T ENSP00000401980.2:n.118-76G>T
NM_001206491.1:c.-132+2818G>T NP_001193420.1:n.-132+2818G>T
NM_020746.4:c.118-76G>T NP_065797.2:n.118-76G>T
NR_037921.1:n.290-76G>T
NM_020746.5:c.118-76G>T MANE Select NP_065797.2:n.118-76G>T
NR_037921.2:n.255-76G>T
NM_001206491.2:c.-132+2818G>T NP_001193420.1:n.-132+2818G>T
NM_001385663.1:c.-430-76G>T NP_001372592.1:n.-430-76G>T