Canonical Allele Identifier: CA2335270580
Gene: SARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38930406T= , CM000681.2:g.38930406T= GRCh38
NC_000019.9:g.39421046T= , CM000681.1:g.39421046T= GRCh37
NC_000019.8:g.44112886T= NCBI36
NG_029222.1:g.4699T=
NG_031865.1:g.5491A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221431.11:c.267+64A= MANE Select ENSP00000221431.6:n.267+64A=
ENST00000221431.10:c.267+64A= ENSP00000221431.5:n.267+64A=
ENST00000430193.7:c.267+64A= ENSP00000406754.3:n.267+64A=
ENST00000455102.6:c.267+64A= ENSP00000414954.2:n.267+64A=
ENST00000593754.1:c.267+64A= ENSP00000471767.1:n.267+64A=
ENST00000598343.5:c.267+64A= ENSP00000472576.1:n.267+64A=
ENST00000598598.5:n.294+64A=
ENST00000599996.1:c.476-4106A=
ENST00000600042.5:c.267+64A= ENSP00000472847.1:n.267+64A=
NM_001145901.1:c.267+64A= NP_001139373.1:n.267+64A=
NM_017827.3:c.267+64A= NP_060297.1:n.267+64A=
NM_001145901.2:c.267+64A= NP_001139373.1:n.267+64A=
NM_017827.4:c.267+64A= MANE Select NP_060297.1:n.267+64A=