Canonical Allele Identifier: CA322799
Gene: SARS2 HGNC NCBI
MRPS12 HGNC NCBI

Linked Data

ClinVar Variation Id: 215114
dbSNP Id: rs145754412

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38930707C>T , CM000681.2:g.38930707C>T GRCh38
NC_000019.9:g.39421347C>T , CM000681.1:g.39421347C>T GRCh37
NC_000019.8:g.44113187C>T NCBI36
NG_029222.1:g.5000C>T
NG_031865.1:g.5190G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000221431.11:c.30G>A (SARS2) MANE Select ENSP00000221431.6:p.Trp10Ter
ENST00000221431.10:c.30G>A (SARS2) ENSP00000221431.5:p.Trp10Ter
ENST00000308018.8:c.-311C>T (MRPS12) ENSP00000308845.3:n.-311C>T
ENST00000430193.7:c.30G>A (SARS2) ENSP00000406754.3:p.Trp10Ter
ENST00000455102.6:c.30G>A (SARS2) ENSP00000414954.2:p.Trp10Ter
ENST00000593754.1:c.30G>A (SARS2) ENSP00000471767.1:p.Trp10Ter
ENST00000598343.5:c.30G>A (SARS2) ENSP00000472576.1:p.Trp10Ter
ENST00000598598.5:n.57G>A (SARS2)
ENST00000599996.1:c.476-4407G>A
ENST00000600042.5:c.30G>A (SARS2) ENSP00000472847.1:p.Trp10Ter
NM_001145901.1:c.30G>A (SARS2) NP_001139373.1:p.Trp10Ter
NM_017827.3:c.30G>A (SARS2) NP_060297.1:p.Trp10Ter
NM_001145901.2:c.30G>A (SARS2) NP_001139373.1:p.Trp10Ter
NM_017827.4:c.30G>A (SARS2) MANE Select NP_060297.1:p.Trp10Ter