Canonical Allele Identifier: CA2768332320
Gene: SLC12A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128186644G>T , CM000667.2:g.128186644G>T GRCh38
NC_000005.9:g.127522336G>T , CM000667.1:g.127522336G>T GRCh37
NC_000005.8:g.127550235G>T NCBI36
NG_042286.1:g.107854G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262461.7:c.*13G>T MANE Select ENSP00000262461.2:n.*13G>T
ENST00000262461.6:c.*13G>T ENSP00000262461.2:n.*13G>T
ENST00000343225.4:c.*13G>T ENSP00000340878.4:n.*13G>T
ENST00000509205.5:c.*265G>T ENSP00000427109.1:n.*265G>T
NM_001046.2:c.*13G>T NP_001037.1:n.*13G>T
NM_001256461.1:c.*13G>T NP_001243390.1:n.*13G>T
NR_046207.1:n.3882G>T
XM_017009771.1:c.*13G>T XP_016865260.1:n.*13G>T
XR_001742214.1:n.3876G>T
NM_001046.3:c.*13G>T MANE Select NP_001037.1:n.*13G>T
NM_001256461.2:c.*13G>T NP_001243390.1:n.*13G>T
NR_046207.2:n.3907G>T