Canonical Allele Identifier: CA10627012

Gene: KCNQ3

Linked Data

• ClinVar Variation Id: 361781
• ClinVar RCV Id: RCV000281222 ; RCV000336242
• dbSNP Id: rs183259250
• gnomAD v2: 8-133135310-G-A
• gnomAD v3: 8-132123063-G-A
• gnomAD v4: 8-132123063-G-A
• MyVariant Identifiers: chr8:g.133135310G>A (hg19) ; chr8:g.132123063G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132123063G>A , CM000670.2:g.132123063G>A	GRCh38
NC_000008.10:g.133135310G>A , CM000670.1:g.133135310G>A	GRCh37
NC_000008.9:g.133204492G>A	NCBI36
NG_008854.2:g.362695C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.*6199C>T MANE Select	ENSP00000373648.3:n.*6199C>T
ENST00000388996.8:c.*6199C>T	ENSP00000373648.3:n.*6199C>T
ENST00000621976.1:c.8455C>T	ENSP00000482510.1:n.8455C>T
NM_001204824.1:c.*6199C>T	NP_001191753.1:n.*6199C>T
NM_004519.3:c.*6199C>T	NP_004510.1:n.*6199C>T
XM_005250914.2:c.*6199C>T	XP_005250971.1:n.*6199C>T
XM_006716555.2:c.*6199C>T	XP_006716618.1:n.*6199C>T
XM_011517026.1:c.*6199C>T	XP_011515328.1:n.*6199C>T
XM_005250914.3:c.*6199C>T	XP_005250971.1:n.*6199C>T
XM_006716555.3:c.*6199C>T	XP_006716618.1:n.*6199C>T
XM_011517026.2:c.*6199C>T	XP_011515328.1:n.*6199C>T
XM_017013400.1:c.*6199C>T	XP_016868889.1:n.*6199C>T
NM_004519.4:c.*6199C>T MANE Select	NP_004510.1:n.*6199C>T
NM_001204824.2:c.*6199C>T	NP_001191753.1:n.*6199C>T