Canonical Allele Identifier: CA507510546

Gene: SARS2 MRPS12

Linked Data

• MyVariant Identifiers: chr19:g.39421230G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930590G>C , CM000681.2:g.38930590G>C	GRCh38
NC_000019.9:g.39421230G>C , CM000681.1:g.39421230G>C	GRCh37
NC_000019.8:g.44113070G>C	NCBI36
NG_029222.1:g.4883G>C
NG_031865.1:g.5307C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.147C>G (SARS2) MANE Select	ENSP00000221431.6:p.Arg49=
ENST00000221431.10:c.147C>G (SARS2)	ENSP00000221431.5:p.Arg49=
ENST00000308018.8:c.-428G>C (MRPS12)	ENSP00000308845.3:n.-428G>C
ENST00000430193.7:c.147C>G (SARS2)	ENSP00000406754.3:p.Arg49=
ENST00000455102.6:c.147C>G (SARS2)	ENSP00000414954.2:p.Arg49=
ENST00000593754.1:c.147C>G (SARS2)	ENSP00000471767.1:p.Arg49=
ENST00000598343.5:c.147C>G (SARS2)	ENSP00000472576.1:p.Arg49=
ENST00000598598.5:n.174C>G (SARS2)
ENST00000599996.1:c.476-4290C>G
ENST00000600042.5:c.147C>G (SARS2)	ENSP00000472847.1:p.Arg49=
NM_001145901.1:c.147C>G (SARS2)	NP_001139373.1:p.Arg49=
NM_017827.3:c.147C>G (SARS2)	NP_060297.1:p.Arg49=
NM_001145901.2:c.147C>G (SARS2)	NP_001139373.1:p.Arg49=
NM_017827.4:c.147C>G (SARS2) MANE Select	NP_060297.1:p.Arg49=