Canonical Allele Identifier: CA658799223
Gene: SARS2 HGNC NCBI
MRPS12 HGNC NCBI

Linked Data

ClinVar Variation Id: 511822
ClinVar RCV Id: RCV000601390
dbSNP Id: rs1464478335

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38930764G>C , CM000681.2:g.38930764G>C GRCh38
NC_000019.9:g.39421404G>C , CM000681.1:g.39421404G>C GRCh37
NC_000019.8:g.44113244G>C NCBI36
NG_029222.1:g.5057G>C
NG_031865.1:g.5133C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221431.10:c.-28C>G (SARS2) ENSP00000221431.5:n.-28C>G
ENST00000308018.8:c.-254G>C (MRPS12) ENSP00000308845.3:n.-254G>C
ENST00000599996.1:c.476-4464C>G
NM_001145901.1:c.-28C>G (SARS2) NP_001139373.1:n.-28C>G
NM_017827.3:c.-28C>G (SARS2) NP_060297.1:n.-28C>G
NM_033362.3:c.-254G>C (MRPS12) NP_203526.1:n.-254G>C