Canonical Allele Identifier: CA308144930
Community Standard Title: NM_017827.4(SARS2):c.535-20C>T
Gene: SARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38921466G>A , CM000681.2:g.38921466G>A GRCh38
NC_000019.9:g.39412106G>A , CM000681.1:g.39412106G>A GRCh37
NC_000019.8:g.44103946G>A NCBI36
NG_031865.1:g.14431C>T

Transcript Alleles

HGVS Amino-acid Change
NM_017827.4:c.535-20C>T MANE Select NP_060297.1:n.535-20C>T
ENST00000221431.11:c.535-20C>T MANE Select ENSP00000221431.6:n.535-20C>T
NM_001145901.1:c.541-20C>T NP_001139373.1:n.541-20C>T
NM_001145901.2:c.541-20C>T NP_001139373.1:n.541-20C>T
NM_017827.3:c.535-20C>T NP_060297.1:n.535-20C>T
ENST00000221431.10:c.535-20C>T ENSP00000221431.5:n.535-20C>T
ENST00000430193.7:c.535-20C>T ENSP00000406754.3:n.535-20C>T
ENST00000455102.6:c.535-20C>T ENSP00000414954.2:n.535-20C>T
ENST00000594171.5:c.-36-20C>T ENSP00000472339.1:n.-36-20C>T
ENST00000598343.5:c.*56-20C>T ENSP00000472576.1:n.*56-20C>T
ENST00000599996.1:c.743-20C>T
ENST00000600042.5:c.541-20C>T ENSP00000472847.1:n.541-20C>T
ENST00000600448.5:n.349-20C>T