Canonical Allele Identifier: CA633276982

Gene: KCNN4

Linked Data

• dbSNP Id: rs1222164121
• gnomAD v2: 19-44280311-A-G
• gnomAD v3: 19-43776159-A-G
• gnomAD v4: 19-43776159-A-G
• MyVariant Identifiers: chr19:g.44280311A>G (hg19) ; chr19:g.43776159A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776159A>G , CM000681.2:g.43776159A>G	GRCh38
NC_000019.9:g.44280311A>G , CM000681.1:g.44280311A>G	GRCh37
NC_000019.8:g.48972151A>G	NCBI36
NG_052672.1:g.10981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+382T>C MANE Select	ENSP00000496939.1:n.255+382T>C
ENST00000262888.7:c.255+382T>C	ENSP00000262888.3:n.255+382T>C
ENST00000599107.1:n.286+382T>C
ENST00000599720.5:c.160-4056T>C	ENSP00000472513.1:n.160-4056T>C
ENST00000615047.4:c.70+382T>C	ENSP00000485014.1:n.70+382T>C
NM_002250.2:c.255+382T>C	NP_002241.1:n.255+382T>C
XM_005258882.2:c.160-1540T>C	XP_005258939.1:n.160-1540T>C
XM_005258883.2:c.70+382T>C	XP_005258940.1:n.70+382T>C
XM_011526938.1:c.255+382T>C	XP_011525240.1:n.255+382T>C
XR_935823.1:n.1533+382T>C
XR_002958313.1:n.1533+382T>C
NM_002250.3:c.255+382T>C MANE Select	NP_002241.1:n.255+382T>C