Canonical Allele Identifier: CA507510511
Gene: SARS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39421164T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38930524T>G , CM000681.2:g.38930524T>G GRCh38
NC_000019.9:g.39421164T>G , CM000681.1:g.39421164T>G GRCh37
NC_000019.8:g.44113004T>G NCBI36
NG_029222.1:g.4817T>G
NG_031865.1:g.5373A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221431.11:c.213A>C MANE Select ENSP00000221431.6:p.Ala71=
ENST00000221431.10:c.213A>C ENSP00000221431.5:p.Ala71=
ENST00000430193.7:c.213A>C ENSP00000406754.3:p.Ala71=
ENST00000455102.6:c.213A>C ENSP00000414954.2:p.Ala71=
ENST00000593754.1:c.213A>C ENSP00000471767.1:p.Ala71=
ENST00000598343.5:c.213A>C ENSP00000472576.1:p.Ala71=
ENST00000598598.5:n.240A>C
ENST00000599996.1:c.476-4224A>C
ENST00000600042.5:c.213A>C ENSP00000472847.1:p.Ala71=
NM_001145901.1:c.213A>C NP_001139373.1:p.Ala71=
NM_017827.3:c.213A>C NP_060297.1:p.Ala71=
NM_001145901.2:c.213A>C NP_001139373.1:p.Ala71=
NM_017827.4:c.213A>C MANE Select NP_060297.1:p.Ala71=