Canonical Allele Identifier: CA360743346

Gene: SLC12A2

Linked Data

• dbSNP Id: rs1763878266
• gnomAD v3: 5-128186611-G-C
• gnomAD v4: 5-128186611-G-C
• MyVariant Identifiers: chr5:g.127522303G>C (hg19) ; chr5:g.128186611G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186611G>C , CM000667.2:g.128186611G>C	GRCh38
NC_000005.9:g.127522303G>C , CM000667.1:g.127522303G>C	GRCh37
NC_000005.8:g.127550202G>C	NCBI36
NG_042286.1:g.107821G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.3619G>C MANE Select	ENSP00000262461.2:p.Val1207Leu
ENST00000262461.6:c.3619G>C	ENSP00000262461.2:p.Val1207Leu
ENST00000343225.4:c.3571G>C	ENSP00000340878.4:p.Val1191Leu
ENST00000509205.5:c.*232G>C	ENSP00000427109.1:n.*232G>C
NM_001046.2:c.3619G>C	NP_001037.1:p.Val1207Leu
NM_001256461.1:c.3571G>C	NP_001243390.1:p.Val1191Leu
NR_046207.1:n.3849G>C
XM_017009771.1:c.1861G>C	XP_016865260.1:p.Val621Leu
XR_001742214.1:n.3843G>C
NM_001046.3:c.3619G>C MANE Select	NP_001037.1:p.Val1207Leu
NM_001256461.2:c.3571G>C	NP_001243390.1:p.Val1191Leu
NR_046207.2:n.3874G>C