Canonical Allele Identifier: CA507510407

Gene: SARS2

Linked Data

• dbSNP Id: rs1373366647
• MyVariant Identifiers: chr19:g.39421113C>A (hg19) ; chr19:g.38930473C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930473C>A , CM000681.2:g.38930473C>A	GRCh38
NC_000019.9:g.39421113C>A , CM000681.1:g.39421113C>A	GRCh37
NC_000019.8:g.44112953C>A	NCBI36
NG_029222.1:g.4766C>A
NG_031865.1:g.5424G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.264G>T MANE Select	ENSP00000221431.6:p.Ala88=
ENST00000221431.10:c.264G>T	ENSP00000221431.5:p.Ala88=
ENST00000430193.7:c.264G>T	ENSP00000406754.3:p.Ala88=
ENST00000455102.6:c.264G>T	ENSP00000414954.2:p.Ala88=
ENST00000593754.1:c.264G>T	ENSP00000471767.1:p.Ala88=
ENST00000598343.5:c.264G>T	ENSP00000472576.1:p.Ala88=
ENST00000598598.5:n.291G>T
ENST00000599996.1:c.476-4173G>T
ENST00000600042.5:c.264G>T	ENSP00000472847.1:p.Ala88=
NM_001145901.1:c.264G>T	NP_001139373.1:p.Ala88=
NM_017827.3:c.264G>T	NP_060297.1:p.Ala88=
NM_001145901.2:c.264G>T	NP_001139373.1:p.Ala88=
NM_017827.4:c.264G>T MANE Select	NP_060297.1:p.Ala88=