Canonical Allele Identifier: CA11702154
Gene: NOCT HGNC NCBI

Linked Data

dbSNP Id: rs17050680

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.139025494A>G , CM000666.2:g.139025494A>G GRCh38
NC_000004.11:g.139946648A>G , CM000666.1:g.139946648A>G GRCh37
NC_000004.10:g.140166098A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000280614.4:c.190+9323A>G MANE Select ENSP00000280614.2:n.190+9323A>G
ENST00000280614.3:c.190+9323A>G ENSP00000280614.2:n.190+9323A>G
ENST00000630479.1:c.190+9323A>G ENSP00000486546.1:n.190+9323A>G
NM_012118.3:c.190+9323A>G NP_036250.2:n.190+9323A>G
NM_012118.4:c.190+9323A>G MANE Select NP_036250.2:n.190+9323A>G