Canonical Allele Identifier: CA308795159

Gene: KCNN4

Linked Data

• dbSNP Id: rs975491803
• gnomAD v3: 19-43776332-G-T
• gnomAD v4: 19-43776332-G-T
• MyVariant Identifiers: chr19:g.44280484G>T (hg19) ; chr19:g.43776332G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776332G>T , CM000681.2:g.43776332G>T	GRCh38
NC_000019.9:g.44280484G>T , CM000681.1:g.44280484G>T	GRCh37
NC_000019.8:g.48972324G>T	NCBI36
NG_052672.1:g.10808C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000648319.1:c.255+209C>A MANE Select	ENSP00000496939.1:n.255+209C>A
ENST00000262888.7:c.255+209C>A	ENSP00000262888.3:n.255+209C>A
ENST00000599107.1:n.286+209C>A
ENST00000599720.5:c.160-4229C>A	ENSP00000472513.1:n.160-4229C>A
ENST00000615047.4:c.70+209C>A	ENSP00000485014.1:n.70+209C>A
NM_002250.2:c.255+209C>A	NP_002241.1:n.255+209C>A
XM_005258882.2:c.160-1713C>A	XP_005258939.1:n.160-1713C>A
XM_005258883.2:c.70+209C>A	XP_005258940.1:n.70+209C>A
XM_011526938.1:c.255+209C>A	XP_011525240.1:n.255+209C>A
XR_935823.1:n.1533+209C>A
XR_002958313.1:n.1533+209C>A
NM_002250.3:c.255+209C>A MANE Select	NP_002241.1:n.255+209C>A