Canonical Allele Identifier: CA308795276

Gene: KCNN4

Linked Data

• dbSNP Id: rs958160966
• MyVariant Identifiers: chr19:g.44280674G>C (hg19) ; chr19:g.43776522G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776522G>C , CM000681.2:g.43776522G>C	GRCh38
NC_000019.9:g.44280674G>C , CM000681.1:g.44280674G>C	GRCh37
NC_000019.8:g.48972514G>C	NCBI36
NG_052672.1:g.10618C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+19C>G MANE Select	ENSP00000496939.1:n.255+19C>G
ENST00000262888.7:c.255+19C>G	ENSP00000262888.3:n.255+19C>G
ENST00000599107.1:n.286+19C>G
ENST00000599720.5:c.159+4181C>G	ENSP00000472513.1:n.159+4181C>G
ENST00000615047.4:c.70+19C>G	ENSP00000485014.1:n.70+19C>G
NM_002250.2:c.255+19C>G	NP_002241.1:n.255+19C>G
XM_005258882.2:c.160-1903C>G	XP_005258939.1:n.160-1903C>G
XM_005258883.2:c.70+19C>G	XP_005258940.1:n.70+19C>G
XM_011526938.1:c.255+19C>G	XP_011525240.1:n.255+19C>G
XR_935823.1:n.1533+19C>G
XR_002958313.1:n.1533+19C>G
NM_002250.3:c.255+19C>G MANE Select	NP_002241.1:n.255+19C>G