Canonical Allele Identifier: CA495613551
Gene: SLC12A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.56938315G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56904403G>C , CM000678.2:g.56904403G>C GRCh38
NC_000016.9:g.56938315G>C , CM000678.1:g.56938315G>C GRCh37
NC_000016.8:g.55495816G>C NCBI36
NG_009386.1:g.44197G>C
NG_009386.2:g.44197G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000563236.6:c.2865G>C MANE Select ENSP00000456149.2:p.Arg955=
ENST00000262502.5:c.2862G>C ENSP00000262502.5:p.Arg954=
ENST00000438926.6:c.2892G>C ENSP00000402152.2:p.Arg964=
ENST00000563236.5:c.2865G>C ENSP00000456149.1:p.Arg955=
ENST00000566786.5:c.2889G>C ENSP00000457552.1:p.Arg963=
ENST00000569002.1:n.296G>C
NM_000339.2:c.2892G>C NP_000330.2:p.Arg964=
NM_001126107.1:c.2889G>C NP_001119579.1:p.Arg963=
NM_001126108.1:c.2865G>C NP_001119580.1:p.Arg955=
XM_005256119.1:c.2862G>C XP_005256176.1:p.Arg954=
XM_005256119.2:c.2862G>C XP_005256176.1:p.Arg954=
NM_000339.3:c.2892G>C NP_000330.3:p.Arg964=
NM_001126107.2:c.2889G>C NP_001119579.2:p.Arg963=
NM_001126108.2:c.2865G>C MANE Select NP_001119580.2:p.Arg955=