Canonical Allele Identifier: CA308149950

Gene: SARS2

Linked Data

• dbSNP Id: rs551059571
• gnomAD v2: 19-39421176-T-C
• gnomAD v3: 19-38930536-T-C
• gnomAD v4: 19-38930536-T-C
• MyVariant Identifiers: chr19:g.39421176T>C (hg19) ; chr19:g.38930536T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930536T>C , CM000681.2:g.38930536T>C	GRCh38
NC_000019.9:g.39421176T>C , CM000681.1:g.39421176T>C	GRCh37
NC_000019.8:g.44113016T>C	NCBI36
NG_029222.1:g.4829T>C
NG_031865.1:g.5361A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.201A>G MANE Select	ENSP00000221431.6:p.Pro67=
ENST00000221431.10:c.201A>G	ENSP00000221431.5:p.Pro67=
ENST00000430193.7:c.201A>G	ENSP00000406754.3:p.Pro67=
ENST00000455102.6:c.201A>G	ENSP00000414954.2:p.Pro67=
ENST00000593754.1:c.201A>G	ENSP00000471767.1:p.Pro67=
ENST00000598343.5:c.201A>G	ENSP00000472576.1:p.Pro67=
ENST00000598598.5:n.228A>G
ENST00000599996.1:c.476-4236A>G
ENST00000600042.5:c.201A>G	ENSP00000472847.1:p.Pro67=
NM_001145901.1:c.201A>G	NP_001139373.1:p.Pro67=
NM_017827.3:c.201A>G	NP_060297.1:p.Pro67=
NM_001145901.2:c.201A>G	NP_001139373.1:p.Pro67=
NM_017827.4:c.201A>G MANE Select	NP_060297.1:p.Pro67=