Canonical Allele Identifier: CA744795684
Gene: KCNS1 HGNC NCBI

Linked Data

dbSNP Id: rs1299142613
MyVariant Identifiers: chr20:g.43721494T>C (hg19) chr20:g.45092853T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45092853T>C , CM000682.2:g.45092853T>C GRCh38
NC_000020.10:g.43721494T>C , CM000682.1:g.43721494T>C GRCh37
NC_000020.9:g.43154908T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537075.3:c.*2017A>G MANE Select ENSP00000445595.1:n.*2017A>G
ENST00000306117.5:c.*2017A>G ENSP00000307694.1:n.*2017A>G
NM_002251.3:c.*2017A>G NP_002242.2:n.*2017A>G
XM_005260409.3:c.*2017A>G XP_005260466.1:n.*2017A>G
NM_001322799.1:c.*2017A>G NP_001309728.1:n.*2017A>G
NM_002251.4:c.*2017A>G NP_002242.2:n.*2017A>G
XM_017027846.1:c.*2017A>G XP_016883335.1:n.*2017A>G
NM_001322799.2:c.*2017A>G MANE Select NP_001309728.1:n.*2017A>G
NM_002251.5:c.*2017A>G NP_002242.2:n.*2017A>G
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