Canonical Allele Identifier: CA405741646

Gene: SARS2

Linked Data

• MyVariant Identifiers: chr19:g.39421150A>T (hg19) ; chr19:g.38930510A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930510A>T , CM000681.2:g.38930510A>T	GRCh38
NC_000019.9:g.39421150A>T , CM000681.1:g.39421150A>T	GRCh37
NC_000019.8:g.44112990A>T	NCBI36
NG_029222.1:g.4803A>T
NG_031865.1:g.5387T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.227T>A MANE Select	ENSP00000221431.6:p.Leu76His
ENST00000221431.10:c.227T>A	ENSP00000221431.5:p.Leu76His
ENST00000430193.7:c.227T>A	ENSP00000406754.3:p.Leu76His
ENST00000455102.6:c.227T>A	ENSP00000414954.2:p.Leu76His
ENST00000593754.1:c.227T>A	ENSP00000471767.1:p.Leu76His
ENST00000598343.5:c.227T>A	ENSP00000472576.1:p.Leu76His
ENST00000598598.5:n.254T>A
ENST00000599996.1:c.476-4210T>A
ENST00000600042.5:c.227T>A	ENSP00000472847.1:p.Leu76His
NM_001145901.1:c.227T>A	NP_001139373.1:p.Leu76His
NM_017827.3:c.227T>A	NP_060297.1:p.Leu76His
NM_001145901.2:c.227T>A	NP_001139373.1:p.Leu76His
NM_017827.4:c.227T>A MANE Select	NP_060297.1:p.Leu76His