Canonical Allele Identifier: CA684137420

Gene: NOS1

Linked Data

• dbSNP Id: rs1208945933
• gnomAD v3: 12-117358013-C-A
• gnomAD v4: 12-117358013-C-A
• MyVariant Identifiers: chr12:g.117795818C>A (hg19) ; chr12:g.117358013C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117358013C>A , CM000674.2:g.117358013C>A	GRCh38
NC_000012.11:g.117795818C>A , CM000674.1:g.117795818C>A	GRCh37
NC_000012.10:g.116280201C>A	NCBI36
NG_011991.2:g.8765G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000317775.11:c.-421+3499G>T MANE Select	ENSP00000320758.6:n.-421+3499G>T
ENST00000317775.10:c.-421+3499G>T	ENSP00000320758.6:n.-421+3499G>T
ENST00000477584.1:n.118+3499G>T
ENST00000549189.1:n.471-26524G>T
ENST00000618760.4:c.-421+3499G>T	ENSP00000477999.1:n.-421+3499G>T
NM_000620.4:c.-421+3499G>T	NP_000611.1:n.-421+3499G>T
NM_001204218.1:c.-421+3499G>T	NP_001191147.1:n.-421+3499G>T
XM_011538398.1:c.-421+978G>T	XP_011536700.1:n.-421+978G>T
NM_000620.5:c.-421+3499G>T MANE Select	NP_000611.1:n.-421+3499G>T
NM_001204218.2:c.-421+3499G>T	NP_001191147.1:n.-421+3499G>T