Canonical Allele Identifier: CA2675110056

Gene: SLC12A2

Linked Data

• gnomAD v4: 5-128186766-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186766C>T , CM000667.2:g.128186766C>T	GRCh38
NC_000005.9:g.127522458C>T , CM000667.1:g.127522458C>T	GRCh37
NC_000005.8:g.127550357C>T	NCBI36
NG_042286.1:g.107976C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262461.7:c.*135C>T MANE Select	ENSP00000262461.2:n.*135C>T
ENST00000262461.6:c.*135C>T	ENSP00000262461.2:n.*135C>T
ENST00000343225.4:c.*135C>T	ENSP00000340878.4:n.*135C>T
ENST00000509205.5:c.*387C>T	ENSP00000427109.1:n.*387C>T
NM_001046.2:c.*135C>T	NP_001037.1:n.*135C>T
NM_001256461.1:c.*135C>T	NP_001243390.1:n.*135C>T
NR_046207.1:n.4004C>T
XM_017009771.1:c.*135C>T	XP_016865260.1:n.*135C>T
XR_001742214.1:n.3998C>T
NM_001046.3:c.*135C>T MANE Select	NP_001037.1:n.*135C>T
NM_001256461.2:c.*135C>T	NP_001243390.1:n.*135C>T
NR_046207.2:n.4029C>T