Canonical Allele Identifier: CA2685613457
Gene: NOS3 HGNC NCBI

Linked Data

gnomAD v4: 7-151011011-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151011011G>T , CM000669.2:g.151011011G>T GRCh38
NC_000007.13:g.150708099G>T , CM000669.1:g.150708099G>T GRCh37
NC_000007.12:g.150339032G>T NCBI36
NG_011992.1:g.24953G>T
NG_030317.1:g.18489C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.2984+25G>T MANE Select ENSP00000297494.3:n.2984+25G>T
ENST00000297494.7:c.2984+25G>T ENSP00000297494.3:n.2984+25G>T
ENST00000461406.5:c.2366+25G>T ENSP00000417143.1:n.2366+25G>T
ENST00000468293.5:n.467+25G>T
ENST00000475017.1:c.865+25G>T
ENST00000477227.1:n.363+25G>T
NM_000603.4:c.2984+25G>T NP_000594.2:n.2984+25G>T
NM_000603.5:c.2984+25G>T MANE Select NP_000594.2:n.2984+25G>T
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