Canonical Allele Identifier: CA137606772
Gene: KCNK5 HGNC NCBI

Linked Data

dbSNP Id: rs1020268915
MyVariant Identifiers: chr6:g.39183688G>C (hg19) chr6:g.39215912G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39215912G>C , CM000668.2:g.39215912G>C GRCh38
NC_000006.11:g.39183688G>C , CM000668.1:g.39183688G>C GRCh37
NC_000006.10:g.39291666G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359534.4:c.186+13014C>G MANE Select ENSP00000352527.3:n.186+13014C>G
ENST00000359534.3:c.186+13014C>G ENSP00000352527.3:n.186+13014C>G
NM_003740.3:c.186+13014C>G NP_003731.1:n.186+13014C>G
XM_005249456.1:c.186+13014C>G XP_005249513.1:n.186+13014C>G
NM_003740.4:c.186+13014C>G MANE Select NP_003731.1:n.186+13014C>G
Search 100 bp 5'
Search 100 bp 3'