Canonical Allele Identifier: CA1000909352
Gene: KCNQ4 HGNC NCBI

Linked Data

dbSNP Id: rs1570792568
gnomAD v3: 1-40783967-C-G
gnomAD v4: 1-40783967-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40783967C>G , CM000663.2:g.40783967C>G GRCh38
NC_000001.10:g.41249639C>G , CM000663.1:g.41249639C>G GRCh37
NC_000001.9:g.41022226C>G NCBI36
NG_008139.1:g.4956C>G
NG_008139.2:g.4956C>G
NG_008139.3:g.5181C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.-127C>G MANE Select ENSP00000262916.6:n.-127C>G
NM_004700.4:c.-127C>G MANE Select NP_004691.2:n.-127C>G
NM_172163.3:c.-127C>G NP_751895.1:n.-127C>G
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