Canonical Allele Identifier: CA446302776

Gene: SLC12A2

Linked Data

• MyVariant Identifiers: chr5:g.127522305C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186613C>G , CM000667.2:g.128186613C>G	GRCh38
NC_000005.9:g.127522305C>G , CM000667.1:g.127522305C>G	GRCh37
NC_000005.8:g.127550204C>G	NCBI36
NG_042286.1:g.107823C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.3621C>G MANE Select	ENSP00000262461.2:p.Val1207=
ENST00000262461.6:c.3621C>G	ENSP00000262461.2:p.Val1207=
ENST00000343225.4:c.3573C>G	ENSP00000340878.4:p.Val1191=
ENST00000509205.5:c.*234C>G	ENSP00000427109.1:n.*234C>G
NM_001046.2:c.3621C>G	NP_001037.1:p.Val1207=
NM_001256461.1:c.3573C>G	NP_001243390.1:p.Val1191=
NR_046207.1:n.3851C>G
XM_017009771.1:c.1863C>G	XP_016865260.1:p.Val621=
XR_001742214.1:n.3845C>G
NM_001046.3:c.3621C>G MANE Select	NP_001037.1:p.Val1207=
NM_001256461.2:c.3573C>G	NP_001243390.1:p.Val1191=
NR_046207.2:n.3876C>G