Canonical Allele Identifier: CA150362941
Gene: NOX3 HGNC NCBI

Linked Data

dbSNP Id: rs755838350
MyVariant Identifiers: chr6:g.155749119C>G (hg19) chr6:g.155427985C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155427985C>G , CM000668.2:g.155427985C>G GRCh38
NC_000006.11:g.155749119C>G , CM000668.1:g.155749119C>G GRCh37
NC_000006.10:g.155790811C>G NCBI36
NG_011995.1:g.32919G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000159060.3:c.1145+809G>C MANE Select ENSP00000159060.2:n.1145+809G>C
ENST00000159060.2:c.1145+809G>C ENSP00000159060.2:n.1145+809G>C
NM_015718.2:c.1145+809G>C NP_056533.1:n.1145+809G>C
NM_015718.3:c.1145+809G>C MANE Select NP_056533.1:n.1145+809G>C
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