Canonical Allele Identifier: CA446302741

Gene: SLC12A2

Linked Data

• MyVariant Identifiers: chr5:g.127522257T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186565T>G , CM000667.2:g.128186565T>G	GRCh38
NC_000005.9:g.127522257T>G , CM000667.1:g.127522257T>G	GRCh37
NC_000005.8:g.127550156T>G	NCBI36
NG_042286.1:g.107775T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.3573T>G MANE Select	ENSP00000262461.2:p.Ser1191=
ENST00000262461.6:c.3573T>G	ENSP00000262461.2:p.Ser1191=
ENST00000343225.4:c.3525T>G	ENSP00000340878.4:p.Ser1175=
ENST00000509205.5:c.*186T>G	ENSP00000427109.1:n.*186T>G
NM_001046.2:c.3573T>G	NP_001037.1:p.Ser1191=
NM_001256461.1:c.3525T>G	NP_001243390.1:p.Ser1175=
NR_046207.1:n.3803T>G
XM_017009771.1:c.1815T>G	XP_016865260.1:p.Ser605=
XR_001742214.1:n.3797T>G
NM_001046.3:c.3573T>G MANE Select	NP_001037.1:p.Ser1191=
NM_001256461.2:c.3525T>G	NP_001243390.1:p.Ser1175=
NR_046207.2:n.3828T>G