Canonical Allele Identifier: CA633068532

Gene: SARS2

Linked Data

• dbSNP Id: rs1568430591
• gnomAD v2: 19-39421062-TC-T
• gnomAD v4: 19-38930422-TC-T
• MyVariant Identifiers: chr19:g.39421063del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930424del , CM000681.2:g.38930424del	GRCh38
NC_000019.9:g.39421064del , CM000681.1:g.39421064del	GRCh37
NC_000019.8:g.44112904del	NCBI36
NG_029222.1:g.4717del
NG_031865.1:g.5474del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.267+47del MANE Select	ENSP00000221431.6:n.267+47del
ENST00000221431.10:c.267+47del	ENSP00000221431.5:n.267+47del
ENST00000430193.7:c.267+47del	ENSP00000406754.3:n.267+47del
ENST00000455102.6:c.267+47del	ENSP00000414954.2:n.267+47del
ENST00000593754.1:c.267+47del	ENSP00000471767.1:n.267+47del
ENST00000598343.5:c.267+47del	ENSP00000472576.1:n.267+47del
ENST00000598598.5:n.294+47del
ENST00000599996.1:c.476-4123del
ENST00000600042.5:c.267+47del	ENSP00000472847.1:n.267+47del
NM_001145901.1:c.267+47del	NP_001139373.1:n.267+47del
NM_017827.3:c.267+47del	NP_060297.1:n.267+47del
NM_001145901.2:c.267+47del	NP_001139373.1:n.267+47del
NM_017827.4:c.267+47del MANE Select	NP_060297.1:n.267+47del