Canonical Allele Identifier: CA405741519

Gene: SARS2

Linked Data

• gnomAD v4: 19-38930478-G-T
• MyVariant Identifiers: chr19:g.39421118G>T (hg19) ; chr19:g.38930478G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930478G>T , CM000681.2:g.38930478G>T	GRCh38
NC_000019.9:g.39421118G>T , CM000681.1:g.39421118G>T	GRCh37
NC_000019.8:g.44112958G>T	NCBI36
NG_029222.1:g.4771G>T
NG_031865.1:g.5419C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.259C>A MANE Select	ENSP00000221431.6:p.Pro87Thr
ENST00000221431.10:c.259C>A	ENSP00000221431.5:p.Pro87Thr
ENST00000430193.7:c.259C>A	ENSP00000406754.3:p.Pro87Thr
ENST00000455102.6:c.259C>A	ENSP00000414954.2:p.Pro87Thr
ENST00000593754.1:c.259C>A	ENSP00000471767.1:p.Pro87Thr
ENST00000598343.5:c.259C>A	ENSP00000472576.1:p.Pro87Thr
ENST00000598598.5:n.286C>A
ENST00000599996.1:c.476-4178C>A
ENST00000600042.5:c.259C>A	ENSP00000472847.1:p.Pro87Thr
NM_001145901.1:c.259C>A	NP_001139373.1:p.Pro87Thr
NM_017827.3:c.259C>A	NP_060297.1:p.Pro87Thr
NM_001145901.2:c.259C>A	NP_001139373.1:p.Pro87Thr
NM_017827.4:c.259C>A MANE Select	NP_060297.1:p.Pro87Thr