Canonical Allele Identifier: CA9750040

Gene: MAVS

Linked Data

• dbSNP Id: rs774495971
• ExAC: 20:3838517 T / C
• gnomAD v2: 20-3838517-T-C
• gnomAD v4: 20-3857870-T-C
• MyVariant Identifiers: chr20:g.3838517T>C (hg19) ; chr20:g.3857870T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857870T>C , CM000682.2:g.3857870T>C	GRCh38
NC_000020.10:g.3838517T>C , CM000682.1:g.3838517T>C	GRCh37
NC_000020.9:g.3786517T>C	NCBI36
NG_030028.1:g.16072T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.292+61T>C MANE Select	ENSP00000401980.2:n.292+61T>C
ENST00000416600.6:c.-132+3129T>C	ENSP00000413749.2:n.-132+3129T>C
ENST00000428216.3:c.292+61T>C	ENSP00000401980.2:n.292+61T>C
NM_001206491.1:c.-132+3129T>C	NP_001193420.1:n.-132+3129T>C
NM_020746.4:c.292+61T>C	NP_065797.2:n.292+61T>C
NR_037921.1:n.464+61T>C
NM_020746.5:c.292+61T>C MANE Select	NP_065797.2:n.292+61T>C
NR_037921.2:n.429+61T>C
NM_001206491.2:c.-132+3129T>C	NP_001193420.1:n.-132+3129T>C
NM_001385663.1:c.-256+61T>C	NP_001372592.1:n.-256+61T>C