Canonical Allele Identifier: CA2576777053

Gene: SARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930451C>G , CM000681.2:g.38930451C>G	GRCh38
NC_000019.9:g.39421091C>G , CM000681.1:g.39421091C>G	GRCh37
NC_000019.8:g.44112931C>G	NCBI36
NG_029222.1:g.4744C>G
NG_031865.1:g.5446G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.267+19G>C MANE Select	ENSP00000221431.6:n.267+19G>C
ENST00000221431.10:c.267+19G>C	ENSP00000221431.5:n.267+19G>C
ENST00000430193.7:c.267+19G>C	ENSP00000406754.3:n.267+19G>C
ENST00000455102.6:c.267+19G>C	ENSP00000414954.2:n.267+19G>C
ENST00000593754.1:c.267+19G>C	ENSP00000471767.1:n.267+19G>C
ENST00000598343.5:c.267+19G>C	ENSP00000472576.1:n.267+19G>C
ENST00000598598.5:n.294+19G>C
ENST00000599996.1:c.476-4151G>C
ENST00000600042.5:c.267+19G>C	ENSP00000472847.1:n.267+19G>C
NM_001145901.1:c.267+19G>C	NP_001139373.1:n.267+19G>C
NM_017827.3:c.267+19G>C	NP_060297.1:n.267+19G>C
NM_001145901.2:c.267+19G>C	NP_001139373.1:n.267+19G>C
NM_017827.4:c.267+19G>C MANE Select	NP_060297.1:n.267+19G>C