Canonical Allele Identifier: CA311065531

Gene: MAVS

Linked Data

• dbSNP Id: rs938416467
• MyVariant Identifiers: chr20:g.3838449C>T (hg19) ; chr20:g.3857802C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857802C>T , CM000682.2:g.3857802C>T	GRCh38
NC_000020.10:g.3838449C>T , CM000682.1:g.3838449C>T	GRCh37
NC_000020.9:g.3786449C>T	NCBI36
NG_030028.1:g.16004C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.285C>T MANE Select	ENSP00000401980.2:p.Tyr95=
ENST00000416600.6:c.-132+3061C>T	ENSP00000413749.2:n.-132+3061C>T
ENST00000428216.3:c.285C>T	ENSP00000401980.2:p.Tyr95=
NM_001206491.1:c.-132+3061C>T	NP_001193420.1:n.-132+3061C>T
NM_020746.4:c.285C>T	NP_065797.2:p.Tyr95=
NR_037921.1:n.457C>T
NM_020746.5:c.285C>T MANE Select	NP_065797.2:p.Tyr95=
NR_037921.2:n.422C>T
NM_001206491.2:c.-132+3061C>T	NP_001193420.1:n.-132+3061C>T
NM_001385663.1:c.-263C>T	NP_001372592.1:n.-263C>T