Canonical Allele Identifier: CA824564886
Gene: KCNK5 HGNC NCBI

Linked Data

dbSNP Id: rs1246578267
MyVariant Identifiers: chr6:g.39183575T>C (hg19) chr6:g.39215799T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39215799T>C , CM000668.2:g.39215799T>C GRCh38
NC_000006.11:g.39183575T>C , CM000668.1:g.39183575T>C GRCh37
NC_000006.10:g.39291553T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359534.4:c.186+13127A>G MANE Select ENSP00000352527.3:n.186+13127A>G
ENST00000359534.3:c.186+13127A>G ENSP00000352527.3:n.186+13127A>G
NM_003740.3:c.186+13127A>G NP_003731.1:n.186+13127A>G
XM_005249456.1:c.186+13127A>G XP_005249513.1:n.186+13127A>G
NM_003740.4:c.186+13127A>G MANE Select NP_003731.1:n.186+13127A>G
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