Canonical Allele Identifier: CA2335270768
Gene: SARS2 HGNC NCBI
MRPS12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38930715G= , CM000681.2:g.38930715G= GRCh38
NC_000019.9:g.39421355G= , CM000681.1:g.39421355G= GRCh37
NC_000019.8:g.44113195G= NCBI36
NG_029222.1:g.5008G=
NG_031865.1:g.5182C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221431.11:c.22C= (SARS2) MANE Select ENSP00000221431.6:p.Arg8=
ENST00000221431.10:c.22C= (SARS2) ENSP00000221431.5:p.Arg8=
ENST00000308018.8:c.-303G= (MRPS12) ENSP00000308845.3:n.-303G=
ENST00000430193.7:c.22C= (SARS2) ENSP00000406754.3:p.Arg8=
ENST00000455102.6:c.22C= (SARS2) ENSP00000414954.2:p.Arg8=
ENST00000593754.1:c.22C= (SARS2) ENSP00000471767.1:p.Arg8=
ENST00000598343.5:c.22C= (SARS2) ENSP00000472576.1:p.Arg8=
ENST00000598598.5:n.49C= (SARS2)
ENST00000599996.1:c.476-4415C=
ENST00000600042.5:c.22C= (SARS2) ENSP00000472847.1:p.Arg8=
NM_001145901.1:c.22C= (SARS2) NP_001139373.1:p.Arg8=
NM_017827.3:c.22C= (SARS2) NP_060297.1:p.Arg8=
NM_033362.3:c.-303G= (MRPS12) NP_203526.1:n.-303G=
NM_001145901.2:c.22C= (SARS2) NP_001139373.1:p.Arg8=
NM_017827.4:c.22C= (SARS2) MANE Select NP_060297.1:p.Arg8=