Canonical Allele Identifier: CA9423321

Gene: SARS2

Linked Data

• dbSNP Id: rs746410668
• ExAC: 19:39421170 C / G
• gnomAD v2: 19-39421170-C-G
• MyVariant Identifiers: chr19:g.39421170C>G (hg19) ; chr19:g.38930530C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930530C>G , CM000681.2:g.38930530C>G	GRCh38
NC_000019.9:g.39421170C>G , CM000681.1:g.39421170C>G	GRCh37
NC_000019.8:g.44113010C>G	NCBI36
NG_029222.1:g.4823C>G
NG_031865.1:g.5367G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.207G>C MANE Select	ENSP00000221431.6:p.Glu69Asp
ENST00000221431.10:c.207G>C	ENSP00000221431.5:p.Glu69Asp
ENST00000430193.7:c.207G>C	ENSP00000406754.3:p.Glu69Asp
ENST00000455102.6:c.207G>C	ENSP00000414954.2:p.Glu69Asp
ENST00000593754.1:c.207G>C	ENSP00000471767.1:p.Glu69Asp
ENST00000598343.5:c.207G>C	ENSP00000472576.1:p.Glu69Asp
ENST00000598598.5:n.234G>C
ENST00000599996.1:c.476-4230G>C
ENST00000600042.5:c.207G>C	ENSP00000472847.1:p.Glu69Asp
NM_001145901.1:c.207G>C	NP_001139373.1:p.Glu69Asp
NM_017827.3:c.207G>C	NP_060297.1:p.Glu69Asp
NM_001145901.2:c.207G>C	NP_001139373.1:p.Glu69Asp
NM_017827.4:c.207G>C MANE Select	NP_060297.1:p.Glu69Asp