Canonical Allele Identifier: CA405742329

Gene: SARS2 MRPS12

Linked Data

• MyVariant Identifiers: chr19:g.39421276A>T (hg19) ; chr19:g.38930636A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930636A>T , CM000681.2:g.38930636A>T	GRCh38
NC_000019.9:g.39421276A>T , CM000681.1:g.39421276A>T	GRCh37
NC_000019.8:g.44113116A>T	NCBI36
NG_029222.1:g.4929A>T
NG_031865.1:g.5261T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.101T>A (SARS2) MANE Select	ENSP00000221431.6:p.Phe34Tyr
ENST00000221431.10:c.101T>A (SARS2)	ENSP00000221431.5:p.Phe34Tyr
ENST00000308018.8:c.-382A>T (MRPS12)	ENSP00000308845.3:n.-382A>T
ENST00000430193.7:c.101T>A (SARS2)	ENSP00000406754.3:p.Phe34Tyr
ENST00000455102.6:c.101T>A (SARS2)	ENSP00000414954.2:p.Phe34Tyr
ENST00000593754.1:c.101T>A (SARS2)	ENSP00000471767.1:p.Phe34Tyr
ENST00000598343.5:c.101T>A (SARS2)	ENSP00000472576.1:p.Phe34Tyr
ENST00000598598.5:n.128T>A (SARS2)
ENST00000599996.1:c.476-4336T>A
ENST00000600042.5:c.101T>A (SARS2)	ENSP00000472847.1:p.Phe34Tyr
NM_001145901.1:c.101T>A (SARS2)	NP_001139373.1:p.Phe34Tyr
NM_017827.3:c.101T>A (SARS2)	NP_060297.1:p.Phe34Tyr
NM_001145901.2:c.101T>A (SARS2)	NP_001139373.1:p.Phe34Tyr
NM_017827.4:c.101T>A (SARS2) MANE Select	NP_060297.1:p.Phe34Tyr