Canonical Allele Identifier: CA405742660

Gene: SARS2 MRPS12

Linked Data

• dbSNP Id: rs1220623136
• gnomAD v2: 19-39421364-T-C
• gnomAD v4: 19-38930724-T-C
• MyVariant Identifiers: chr19:g.39421364T>C (hg19) ; chr19:g.38930724T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930724T>C , CM000681.2:g.38930724T>C	GRCh38
NC_000019.9:g.39421364T>C , CM000681.1:g.39421364T>C	GRCh37
NC_000019.8:g.44113204T>C	NCBI36
NG_029222.1:g.5017T>C
NG_031865.1:g.5173A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.13A>G (SARS2) MANE Select	ENSP00000221431.6:p.Met5Val
ENST00000221431.10:c.13A>G (SARS2)	ENSP00000221431.5:p.Met5Val
ENST00000308018.8:c.-294T>C (MRPS12)	ENSP00000308845.3:n.-294T>C
ENST00000430193.7:c.13A>G (SARS2)	ENSP00000406754.3:p.Met5Val
ENST00000455102.6:c.13A>G (SARS2)	ENSP00000414954.2:p.Met5Val
ENST00000593754.1:c.13A>G (SARS2)	ENSP00000471767.1:p.Met5Val
ENST00000598343.5:c.13A>G (SARS2)	ENSP00000472576.1:p.Met5Val
ENST00000598598.5:n.40A>G (SARS2)
ENST00000599996.1:c.476-4424A>G
ENST00000600042.5:c.13A>G (SARS2)	ENSP00000472847.1:p.Met5Val
NM_001145901.1:c.13A>G (SARS2)	NP_001139373.1:p.Met5Val
NM_017827.3:c.13A>G (SARS2)	NP_060297.1:p.Met5Val
NM_033362.3:c.-294T>C (MRPS12)	NP_203526.1:n.-294T>C
NM_001145901.2:c.13A>G (SARS2)	NP_001139373.1:p.Met5Val
NM_017827.4:c.13A>G (SARS2) MANE Select	NP_060297.1:p.Met5Val