Canonical Allele Identifier: CA735772264
Gene: KCNQ4 HGNC NCBI

Linked Data

dbSNP Id: rs1271194772
MyVariant Identifiers: chr1:g.41249714C>G (hg19) chr1:g.40784042C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40784042C>G , CM000663.2:g.40784042C>G GRCh38
NC_000001.10:g.41249714C>G , CM000663.1:g.41249714C>G GRCh37
NC_000001.9:g.41022301C>G NCBI36
NG_008139.1:g.5031C>G
NG_008139.2:g.5031C>G
NG_008139.3:g.5256C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.-52C>G MANE Select ENSP00000262916.6:n.-52C>G
ENST00000347132.9:c.-52C>G ENSP00000262916.6:n.-52C>G
NM_004700.3:c.-52C>G NP_004691.2:n.-52C>G
NM_172163.2:c.-52C>G NP_751895.1:n.-52C>G
NM_004700.4:c.-52C>G MANE Select NP_004691.2:n.-52C>G
NM_172163.3:c.-52C>G NP_751895.1:n.-52C>G
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