Canonical Allele Identifier: CA200465960
Gene: NCS1 HGNC NCBI

Linked Data

dbSNP Id: rs905196905
MyVariant Identifiers: chr9:g.130205013T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130205013T>C , CM000671.2:g.130205013T>C GRCh38
NC_000009.11:g.132967292T>C , CM000671.1:g.132967292T>C GRCh37
NC_000009.10:g.132007113T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000372398.6:c.89+4031T>C MANE Select ENSP00000361475.3:n.89+4031T>C
ENST00000372398.5:c.89+4031T>C ENSP00000361475.3:n.89+4031T>C
ENST00000493042.1:n.143+4031T>C
ENST00000630865.1:c.35+4031T>C ENSP00000486695.1:n.35+4031T>C
NM_001128826.1:c.35+4031T>C NP_001122298.1:n.35+4031T>C
NM_014286.3:c.89+4031T>C NP_055101.2:n.89+4031T>C
NM_014286.4:c.89+4031T>C MANE Select NP_055101.2:n.89+4031T>C
NM_001128826.2:c.35+4031T>C NP_001122298.1:n.35+4031T>C
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