Canonical Allele Identifier: CA405741529

Gene: SARS2

Linked Data

• dbSNP Id: rs1380593052
• gnomAD v2: 19-39421121-G-C
• gnomAD v4: 19-38930481-G-C
• MyVariant Identifiers: chr19:g.39421121G>C (hg19) ; chr19:g.38930481G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930481G>C , CM000681.2:g.38930481G>C	GRCh38
NC_000019.9:g.39421121G>C , CM000681.1:g.39421121G>C	GRCh37
NC_000019.8:g.44112961G>C	NCBI36
NG_029222.1:g.4774G>C
NG_031865.1:g.5416C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.256C>G MANE Select	ENSP00000221431.6:p.Leu86Val
ENST00000221431.10:c.256C>G	ENSP00000221431.5:p.Leu86Val
ENST00000430193.7:c.256C>G	ENSP00000406754.3:p.Leu86Val
ENST00000455102.6:c.256C>G	ENSP00000414954.2:p.Leu86Val
ENST00000593754.1:c.256C>G	ENSP00000471767.1:p.Leu86Val
ENST00000598343.5:c.256C>G	ENSP00000472576.1:p.Leu86Val
ENST00000598598.5:n.283C>G
ENST00000599996.1:c.476-4181C>G
ENST00000600042.5:c.256C>G	ENSP00000472847.1:p.Leu86Val
NM_001145901.1:c.256C>G	NP_001139373.1:p.Leu86Val
NM_017827.3:c.256C>G	NP_060297.1:p.Leu86Val
NM_001145901.2:c.256C>G	NP_001139373.1:p.Leu86Val
NM_017827.4:c.256C>G MANE Select	NP_060297.1:p.Leu86Val