Canonical Allele Identifier: CA1881105067
Gene: NCS1 HGNC NCBI

Linked Data

dbSNP Id: rs1588117297

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130205063G>T , CM000671.2:g.130205063G>T GRCh38
NC_000009.11:g.132967342G>T , CM000671.1:g.132967342G>T GRCh37
NC_000009.10:g.132007163G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000372398.6:c.89+4081G>T MANE Select ENSP00000361475.3:n.89+4081G>T
ENST00000372398.5:c.89+4081G>T ENSP00000361475.3:n.89+4081G>T
ENST00000493042.1:n.143+4081G>T
ENST00000630865.1:c.35+4081G>T ENSP00000486695.1:n.35+4081G>T
NM_001128826.1:c.35+4081G>T NP_001122298.1:n.35+4081G>T
NM_014286.3:c.89+4081G>T NP_055101.2:n.89+4081G>T
NM_014286.4:c.89+4081G>T MANE Select NP_055101.2:n.89+4081G>T
NM_001128826.2:c.35+4081G>T NP_001122298.1:n.35+4081G>T