Canonical Allele Identifier: CA2685613449
Gene: NOS3 HGNC NCBI

Linked Data

gnomAD v4: 7-151011008-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151011008G>C , CM000669.2:g.151011008G>C GRCh38
NC_000007.13:g.150708096G>C , CM000669.1:g.150708096G>C GRCh37
NC_000007.12:g.150339029G>C NCBI36
NG_011992.1:g.24950G>C
NG_030317.1:g.18492C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.2984+22G>C MANE Select ENSP00000297494.3:n.2984+22G>C
ENST00000297494.7:c.2984+22G>C ENSP00000297494.3:n.2984+22G>C
ENST00000461406.5:c.2366+22G>C ENSP00000417143.1:n.2366+22G>C
ENST00000468293.5:n.467+22G>C
ENST00000475017.1:c.865+22G>C
ENST00000477227.1:n.363+22G>C
NM_000603.4:c.2984+22G>C NP_000594.2:n.2984+22G>C
NM_000603.5:c.2984+22G>C MANE Select NP_000594.2:n.2984+22G>C
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