Canonical Allele Identifier: CA200465965

Gene: NCS1

Linked Data

• dbSNP Id: rs1035526189
• gnomAD v3: 9-130205034-G-T
• gnomAD v4: 9-130205034-G-T
• MyVariant Identifiers: chr9:g.130205034G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130205034G>T , CM000671.2:g.130205034G>T	GRCh38
NC_000009.11:g.132967313G>T , CM000671.1:g.132967313G>T	GRCh37
NC_000009.10:g.132007134G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372398.6:c.89+4052G>T MANE Select	ENSP00000361475.3:n.89+4052G>T
ENST00000372398.5:c.89+4052G>T	ENSP00000361475.3:n.89+4052G>T
ENST00000493042.1:n.143+4052G>T
ENST00000630865.1:c.35+4052G>T	ENSP00000486695.1:n.35+4052G>T
NM_001128826.1:c.35+4052G>T	NP_001122298.1:n.35+4052G>T
NM_014286.3:c.89+4052G>T	NP_055101.2:n.89+4052G>T
NM_014286.4:c.89+4052G>T MANE Select	NP_055101.2:n.89+4052G>T
NM_001128826.2:c.35+4052G>T	NP_001122298.1:n.35+4052G>T