Canonical Allele Identifier: CA633068536

Gene: SARS2

Linked Data

• dbSNP Id: rs777004810
• gnomAD v2: 19-39421076-G-C
• gnomAD v4: 19-38930436-G-C
• MyVariant Identifiers: chr19:g.39421076G>C (hg19) ; chr19:g.38930436G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930436G>C , CM000681.2:g.38930436G>C	GRCh38
NC_000019.9:g.39421076G>C , CM000681.1:g.39421076G>C	GRCh37
NC_000019.8:g.44112916G>C	NCBI36
NG_029222.1:g.4729G>C
NG_031865.1:g.5461C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.267+34C>G MANE Select	ENSP00000221431.6:n.267+34C>G
ENST00000221431.10:c.267+34C>G	ENSP00000221431.5:n.267+34C>G
ENST00000430193.7:c.267+34C>G	ENSP00000406754.3:n.267+34C>G
ENST00000455102.6:c.267+34C>G	ENSP00000414954.2:n.267+34C>G
ENST00000593754.1:c.267+34C>G	ENSP00000471767.1:n.267+34C>G
ENST00000598343.5:c.267+34C>G	ENSP00000472576.1:n.267+34C>G
ENST00000598598.5:n.294+34C>G
ENST00000599996.1:c.476-4136C>G
ENST00000600042.5:c.267+34C>G	ENSP00000472847.1:n.267+34C>G
NM_001145901.1:c.267+34C>G	NP_001139373.1:n.267+34C>G
NM_017827.3:c.267+34C>G	NP_060297.1:n.267+34C>G
NM_001145901.2:c.267+34C>G	NP_001139373.1:n.267+34C>G
NM_017827.4:c.267+34C>G MANE Select	NP_060297.1:n.267+34C>G