Canonical Allele Identifier: CA408119164

Gene: MAVS

Linked Data

• dbSNP Id: rs1212230200
• gnomAD v3: 20-3857792-A-G
• gnomAD v4: 20-3857792-A-G
• MyVariant Identifiers: chr20:g.3838439A>G (hg19) ; chr20:g.3857792A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857792A>G , CM000682.2:g.3857792A>G	GRCh38
NC_000020.10:g.3838439A>G , CM000682.1:g.3838439A>G	GRCh37
NC_000020.9:g.3786439A>G	NCBI36
NG_030028.1:g.15994A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.275A>G MANE Select	ENSP00000401980.2:p.Tyr92Cys
ENST00000416600.6:c.-132+3051A>G	ENSP00000413749.2:n.-132+3051A>G
ENST00000428216.3:c.275A>G	ENSP00000401980.2:p.Tyr92Cys
NM_001206491.1:c.-132+3051A>G	NP_001193420.1:n.-132+3051A>G
NM_020746.4:c.275A>G	NP_065797.2:p.Tyr92Cys
NR_037921.1:n.447A>G
NM_020746.5:c.275A>G MANE Select	NP_065797.2:p.Tyr92Cys
NR_037921.2:n.412A>G
NM_001206491.2:c.-132+3051A>G	NP_001193420.1:n.-132+3051A>G
NM_001385663.1:c.-273A>G	NP_001372592.1:n.-273A>G