Canonical Allele Identifier: CA2743310919
Gene: KCNQ4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40783998T>G , CM000663.2:g.40783998T>G GRCh38
NC_000001.10:g.41249670T>G , CM000663.1:g.41249670T>G GRCh37
NC_000001.9:g.41022257T>G NCBI36
NG_008139.1:g.4987T>G
NG_008139.2:g.4987T>G
NG_008139.3:g.5212T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.-96T>G MANE Select ENSP00000262916.6:n.-96T>G
NM_004700.4:c.-96T>G MANE Select NP_004691.2:n.-96T>G
NM_172163.3:c.-96T>G NP_751895.1:n.-96T>G
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