Canonical Allele Identifier: CA2675110038

Gene: SLC12A2

Linked Data

• gnomAD v4: 5-128186740-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186740T>G , CM000667.2:g.128186740T>G	GRCh38
NC_000005.9:g.127522432T>G , CM000667.1:g.127522432T>G	GRCh37
NC_000005.8:g.127550331T>G	NCBI36
NG_042286.1:g.107950T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.*109T>G MANE Select	ENSP00000262461.2:n.*109T>G
ENST00000262461.6:c.*109T>G	ENSP00000262461.2:n.*109T>G
ENST00000343225.4:c.*109T>G	ENSP00000340878.4:n.*109T>G
ENST00000509205.5:c.*361T>G	ENSP00000427109.1:n.*361T>G
NM_001046.2:c.*109T>G	NP_001037.1:n.*109T>G
NM_001256461.1:c.*109T>G	NP_001243390.1:n.*109T>G
NR_046207.1:n.3978T>G
XM_017009771.1:c.*109T>G	XP_016865260.1:n.*109T>G
XR_001742214.1:n.3972T>G
NM_001046.3:c.*109T>G MANE Select	NP_001037.1:n.*109T>G
NM_001256461.2:c.*109T>G	NP_001243390.1:n.*109T>G
NR_046207.2:n.4003T>G