Canonical Allele Identifier: CA2736356083
Gene: MAVS HGNC NCBI

Linked Data

dbSNP Id: rs2146765110

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857556C>T , CM000682.2:g.3857556C>T GRCh38
NC_000020.10:g.3838203C>T , CM000682.1:g.3838203C>T GRCh37
NC_000020.9:g.3786203C>T NCBI36
NG_030028.1:g.15758C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.118-79C>T MANE Select ENSP00000401980.2:n.118-79C>T
ENST00000416600.6:c.-132+2815C>T ENSP00000413749.2:n.-132+2815C>T
ENST00000428216.3:c.118-79C>T ENSP00000401980.2:n.118-79C>T
NM_001206491.1:c.-132+2815C>T NP_001193420.1:n.-132+2815C>T
NM_020746.4:c.118-79C>T NP_065797.2:n.118-79C>T
NR_037921.1:n.290-79C>T
NM_020746.5:c.118-79C>T MANE Select NP_065797.2:n.118-79C>T
NR_037921.2:n.255-79C>T
NM_001206491.2:c.-132+2815C>T NP_001193420.1:n.-132+2815C>T
NM_001385663.1:c.-430-79C>T NP_001372592.1:n.-430-79C>T