Canonical Allele Identifier: CA2651759261
Gene: MAVS HGNC NCBI

Linked Data

gnomAD v4: 20-3857846-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857846C>T , CM000682.2:g.3857846C>T GRCh38
NC_000020.10:g.3838493C>T , CM000682.1:g.3838493C>T GRCh37
NC_000020.9:g.3786493C>T NCBI36
NG_030028.1:g.16048C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.292+37C>T MANE Select ENSP00000401980.2:n.292+37C>T
ENST00000416600.6:c.-132+3105C>T ENSP00000413749.2:n.-132+3105C>T
ENST00000428216.3:c.292+37C>T ENSP00000401980.2:n.292+37C>T
NM_001206491.1:c.-132+3105C>T NP_001193420.1:n.-132+3105C>T
NM_020746.4:c.292+37C>T NP_065797.2:n.292+37C>T
NR_037921.1:n.464+37C>T
NM_020746.5:c.292+37C>T MANE Select NP_065797.2:n.292+37C>T
NR_037921.2:n.429+37C>T
NM_001206491.2:c.-132+3105C>T NP_001193420.1:n.-132+3105C>T
NM_001385663.1:c.-256+37C>T NP_001372592.1:n.-256+37C>T