Canonical Allele Identifier: CA311065316

Gene: MAVS

Linked Data

• dbSNP Id: rs984679015
• gnomAD v2: 20-3838376-A-G
• gnomAD v4: 20-3857729-A-G
• MyVariant Identifiers: chr20:g.3838376A>G (hg19) ; chr20:g.3857729A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857729A>G , CM000682.2:g.3857729A>G	GRCh38
NC_000020.10:g.3838376A>G , CM000682.1:g.3838376A>G	GRCh37
NC_000020.9:g.3786376A>G	NCBI36
NG_030028.1:g.15931A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.212A>G MANE Select	ENSP00000401980.2:p.Tyr71Cys
ENST00000416600.6:c.-132+2988A>G	ENSP00000413749.2:n.-132+2988A>G
ENST00000428216.3:c.212A>G	ENSP00000401980.2:p.Tyr71Cys
NM_001206491.1:c.-132+2988A>G	NP_001193420.1:n.-132+2988A>G
NM_020746.4:c.212A>G	NP_065797.2:p.Tyr71Cys
NR_037921.1:n.384A>G
NM_020746.5:c.212A>G MANE Select	NP_065797.2:p.Tyr71Cys
NR_037921.2:n.349A>G
NM_001206491.2:c.-132+2988A>G	NP_001193420.1:n.-132+2988A>G
NM_001385663.1:c.-336A>G	NP_001372592.1:n.-336A>G