Canonical Allele Identifier: CA2645130537
Gene: KCNQ4 HGNC NCBI

Linked Data

gnomAD v4: 1-40783996-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40783996T>A , CM000663.2:g.40783996T>A GRCh38
NC_000001.10:g.41249668T>A , CM000663.1:g.41249668T>A GRCh37
NC_000001.9:g.41022255T>A NCBI36
NG_008139.1:g.4985T>A
NG_008139.2:g.4985T>A
NG_008139.3:g.5210T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.-98T>A MANE Select ENSP00000262916.6:n.-98T>A
NM_004700.4:c.-98T>A MANE Select NP_004691.2:n.-98T>A
NM_172163.3:c.-98T>A NP_751895.1:n.-98T>A