Canonical Allele Identifier: CA406968299

Gene: KCNC3

Linked Data

• dbSNP Id: rs746943393
• gnomAD v3: 19-50320599-G-C
• gnomAD v4: 19-50320599-G-C
• MyVariant Identifiers: chr19:g.50823856G>C (hg19) ; chr19:g.50320599G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50320599G>C , CM000681.2:g.50320599G>C	GRCh38
NC_000019.9:g.50823856G>C , CM000681.1:g.50823856G>C	GRCh37
NC_000019.8:g.55515668G>C	NCBI36
NG_008134.2:g.13779C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000477616.2:c.2164C>G MANE Select	ENSP00000434241.1:p.Arg722Gly
ENST00000670667.1:c.2164C>G	ENSP00000499301.1:p.Arg722Gly
ENST00000376959.6:c.2164C>G	ENSP00000366158.2:p.Arg722Gly
ENST00000474951.1:c.112C>G	ENSP00000432438.1:p.Arg38Gly
ENST00000477616.1:c.2164C>G	ENSP00000434241.1:p.Arg722Gly
NM_004977.2:c.2164C>G	NP_004968.2:p.Arg722Gly
NR_110912.1:n.233C>G
XM_006723203.2:c.2164C>G	XP_006723266.1:p.Arg722Gly
XM_011526925.1:c.2164C>G	XP_011525227.1:p.Arg722Gly
XM_011526926.1:c.2164C>G	XP_011525228.1:p.Arg722Gly
XM_011526927.1:c.2164C>G	XP_011525229.1:p.Arg722Gly
XM_011526928.1:c.2164C>G	XP_011525230.1:p.Arg722Gly
NM_001372305.1:c.1936C>G	NP_001359234.1:p.Arg646Gly
NM_004977.3:c.2164C>G MANE Select	NP_004968.2:p.Arg722Gly
NR_110912.2:n.254C>G