Canonical Allele Identifier: CA9749992

Gene: MAVS

Linked Data

• ClinVar Variation Id: 782663
• ClinVar RCV Id: RCV000964082
• dbSNP Id: rs11905658
• ExAC: 20:3838362 C / T
• gnomAD v2: 20-3838362-C-T
• gnomAD v3: 20-3857715-C-T
• gnomAD v4: 20-3857715-C-T
• MyVariant Identifiers: chr20:g.3838362C>T (hg19) ; chr20:g.3857715C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857715C>T , CM000682.2:g.3857715C>T	GRCh38
NC_000020.10:g.3838362C>T , CM000682.1:g.3838362C>T	GRCh37
NC_000020.9:g.3786362C>T	NCBI36
NG_030028.1:g.15917C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.198C>T MANE Select	ENSP00000401980.2:p.Pro66=
ENST00000416600.6:c.-132+2974C>T	ENSP00000413749.2:n.-132+2974C>T
ENST00000428216.3:c.198C>T	ENSP00000401980.2:p.Pro66=
NM_001206491.1:c.-132+2974C>T	NP_001193420.1:n.-132+2974C>T
NM_020746.4:c.198C>T	NP_065797.2:p.Pro66=
NR_037921.1:n.370C>T
NM_020746.5:c.198C>T MANE Select	NP_065797.2:p.Pro66=
NR_037921.2:n.335C>T
NM_001206491.2:c.-132+2974C>T	NP_001193420.1:n.-132+2974C>T
NM_001385663.1:c.-350C>T	NP_001372592.1:n.-350C>T