Canonical Allele Identifier: CA1881104920

Gene: NCS1

Linked Data

• dbSNP Id: rs1833005285

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130204955G>T , CM000671.2:g.130204955G>T	GRCh38
NC_000009.11:g.132967234G>T , CM000671.1:g.132967234G>T	GRCh37
NC_000009.10:g.132007055G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000372398.6:c.89+3973G>T MANE Select	ENSP00000361475.3:n.89+3973G>T
ENST00000372398.5:c.89+3973G>T	ENSP00000361475.3:n.89+3973G>T
ENST00000493042.1:n.143+3973G>T
ENST00000630865.1:c.35+3973G>T	ENSP00000486695.1:n.35+3973G>T
NM_001128826.1:c.35+3973G>T	NP_001122298.1:n.35+3973G>T
NM_014286.3:c.89+3973G>T	NP_055101.2:n.89+3973G>T
NM_014286.4:c.89+3973G>T MANE Select	NP_055101.2:n.89+3973G>T
NM_001128826.2:c.35+3973G>T	NP_001122298.1:n.35+3973G>T