Canonical Allele Identifier: CA9423125
Gene: SARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 329219
ClinVar RCV Id: RCV000315615 RCV000905875
dbSNP Id: rs772644235
ExAC: 19:39412028 C / T
gnomAD v2: 19-39412028-C-T
gnomAD v3: 19-38921388-C-T
gnomAD v4: 19-38921388-C-T
MyVariant Identifiers: chr19:g.39412028C>T (hg19) chr19:g.38921388C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38921388C>T , CM000681.2:g.38921388C>T GRCh38
NC_000019.9:g.39412028C>T , CM000681.1:g.39412028C>T GRCh37
NC_000019.8:g.44103868C>T NCBI36
NG_031865.1:g.14509G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000221431.11:c.589+4G>A MANE Select ENSP00000221431.6:n.589+4G>A
ENST00000221431.10:c.589+4G>A ENSP00000221431.5:n.589+4G>A
ENST00000430193.7:c.589+4G>A ENSP00000406754.3:n.589+4G>A
ENST00000455102.6:c.589+4G>A ENSP00000414954.2:n.589+4G>A
ENST00000594171.5:c.19+4G>A ENSP00000472339.1:n.19+4G>A
ENST00000599996.1:c.797+4G>A
ENST00000600042.5:c.595+4G>A ENSP00000472847.1:n.595+4G>A
ENST00000600448.5:n.403+4G>A
NM_001145901.1:c.595+4G>A NP_001139373.1:n.595+4G>A
NM_017827.3:c.589+4G>A NP_060297.1:n.589+4G>A
NM_001145901.2:c.595+4G>A NP_001139373.1:n.595+4G>A
NM_017827.4:c.589+4G>A MANE Select NP_060297.1:n.589+4G>A
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