Canonical Allele Identifier: CA366342104
Gene: SLC22A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.160668299A>T (hg19) chr6:g.160247267A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160247267A>T , CM000668.2:g.160247267A>T GRCh38
NC_000006.11:g.160668299A>T , CM000668.1:g.160668299A>T GRCh37
NC_000006.10:g.160588289A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366953.8:c.874T>A MANE Select ENSP00000355920.3:p.Ser292Thr
ENST00000366952.1:c.811T>A ENSP00000355919.1:p.Ser271Thr
ENST00000366953.7:c.874T>A ENSP00000355920.3:p.Ser292Thr
ENST00000491092.1:n.771T>A
NM_003058.3:c.874T>A NP_003049.2:p.Ser292Thr
NM_003058.4:c.874T>A MANE Select NP_003049.2:p.Ser292Thr
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