Canonical Allele Identifier: CA835224087
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1360821004
gnomAD v3: 7-150992970-G-C
gnomAD v4: 7-150992970-G-C
MyVariant Identifiers: chr7:g.150690058G>C (hg19) chr7:g.150992970G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992970G>C , CM000669.2:g.150992970G>C GRCh38
NC_000007.13:g.150690058G>C , CM000669.1:g.150690058G>C GRCh37
NC_000007.12:g.150320991G>C NCBI36
NG_011992.1:g.6912G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.-51-783G>C MANE Select ENSP00000297494.3:n.-51-783G>C
ENST00000297494.7:c.-51-783G>C ENSP00000297494.3:n.-51-783G>C
ENST00000461406.5:c.-149+1670G>C ENSP00000417143.1:n.-149+1670G>C
NM_000603.4:c.-51-783G>C NP_000594.2:n.-51-783G>C
NM_000603.5:c.-51-783G>C MANE Select NP_000594.2:n.-51-783G>C
Search 100 bp 5'
Search 100 bp 3'