Canonical Allele Identifier: CA137606741
Gene: KCNK5 HGNC NCBI

Linked Data

dbSNP Id: rs570989074
gnomAD v2: 6-39183663-T-C
gnomAD v3: 6-39215887-T-C
gnomAD v4: 6-39215887-T-C
MyVariant Identifiers: chr6:g.39183663T>C (hg19) chr6:g.39215887T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39215887T>C , CM000668.2:g.39215887T>C GRCh38
NC_000006.11:g.39183663T>C , CM000668.1:g.39183663T>C GRCh37
NC_000006.10:g.39291641T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359534.4:c.186+13039A>G MANE Select ENSP00000352527.3:n.186+13039A>G
ENST00000359534.3:c.186+13039A>G ENSP00000352527.3:n.186+13039A>G
NM_003740.3:c.186+13039A>G NP_003731.1:n.186+13039A>G
XM_005249456.1:c.186+13039A>G XP_005249513.1:n.186+13039A>G
NM_003740.4:c.186+13039A>G MANE Select NP_003731.1:n.186+13039A>G
Search 100 bp 5'
Search 100 bp 3'