Canonical Allele Identifier: CA9423302

Gene: SARS2

Linked Data

• dbSNP Id: rs771376102
• ExAC: 19:39421123 T / C
• gnomAD v2: 19-39421123-T-C
• gnomAD v4: 19-38930483-T-C
• COSMIC: COSM5807169 ; COSM5807170
• MyVariant Identifiers: chr19:g.39421123T>C (hg19) ; chr19:g.38930483T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930483T>C , CM000681.2:g.38930483T>C	GRCh38
NC_000019.9:g.39421123T>C , CM000681.1:g.39421123T>C	GRCh37
NC_000019.8:g.44112963T>C	NCBI36
NG_029222.1:g.4776T>C
NG_031865.1:g.5414A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.254A>G MANE Select	ENSP00000221431.6:p.Asp85Gly
ENST00000221431.10:c.254A>G	ENSP00000221431.5:p.Asp85Gly
ENST00000430193.7:c.254A>G	ENSP00000406754.3:p.Asp85Gly
ENST00000455102.6:c.254A>G	ENSP00000414954.2:p.Asp85Gly
ENST00000593754.1:c.254A>G	ENSP00000471767.1:p.Asp85Gly
ENST00000598343.5:c.254A>G	ENSP00000472576.1:p.Asp85Gly
ENST00000598598.5:n.281A>G
ENST00000599996.1:c.476-4183A>G
ENST00000600042.5:c.254A>G	ENSP00000472847.1:p.Asp85Gly
NM_001145901.1:c.254A>G	NP_001139373.1:p.Asp85Gly
NM_017827.3:c.254A>G	NP_060297.1:p.Asp85Gly
NM_001145901.2:c.254A>G	NP_001139373.1:p.Asp85Gly
NM_017827.4:c.254A>G MANE Select	NP_060297.1:p.Asp85Gly