Canonical Allele Identifier: CA9422779
Gene: SARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 329211
ClinVar RCV Id: RCV000290523
dbSNP Id: rs762422369
ExAC: 19:39406703 C / T
gnomAD v2: 19-39406703-C-T
gnomAD v3: 19-38916063-C-T
gnomAD v4: 19-38916063-C-T
MyVariant Identifiers: chr19:g.39406703C>T (hg19) chr19:g.38916063C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38916063C>T , CM000681.2:g.38916063C>T GRCh38
NC_000019.9:g.39406703C>T , CM000681.1:g.39406703C>T GRCh37
NC_000019.8:g.44098543C>T NCBI36
NG_031865.1:g.19834G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000221431.11:c.1321G>A MANE Select ENSP00000221431.6:p.Ala441Thr
ENST00000221431.10:c.1321G>A ENSP00000221431.5:p.Ala441Thr
ENST00000430193.7:c.1321G>A ENSP00000406754.3:p.Ala441Thr
ENST00000594171.5:c.751G>A ENSP00000472339.1:p.Ala251Thr
ENST00000598831.5:c.265G>A ENSP00000468865.1:p.Ala89Thr
ENST00000599996.1:c.1529G>A
ENST00000600042.5:c.1327G>A ENSP00000472847.1:p.Ala443Thr
NM_001145901.1:c.1327G>A NP_001139373.1:p.Ala443Thr
NM_017827.3:c.1321G>A NP_060297.1:p.Ala441Thr
NM_001145901.2:c.1327G>A NP_001139373.1:p.Ala443Thr
NM_017827.4:c.1321G>A MANE Select NP_060297.1:p.Ala441Thr
Search 100 bp 5'
Search 100 bp 3'