Canonical Allele Identifier: CA1948160092
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444779A= , CM000673.2:g.2444779A= GRCh38
NC_000011.9:g.2466009A= , CM000673.1:g.2466009A= GRCh37
NC_000011.8:g.2422585A= NCBI36
NG_008935.1:g.4789A= , LRG_287:g.4789A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.23+71A= ENSP00000434560.2:n.23+71A=
ENST00000496887.6:c.23+71A= ENSP00000434560.1:n.23+71A=