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ClinGen Allele Registry
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Canonical Allele Identifier:
CA1676974871
Community Standard Title: NM_003058.4(SLC22A2):c.808T= (p.Ser270=)
Gene: SLC22A2
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.160249250A= , CM000668.2:g.160249250A=
GRCh38
NC_000006.11:g.160670282A= , CM000668.1:g.160670282A=
GRCh37
NC_000006.10:g.160590272A=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NM_003058.4:c.808T=
MANE Select
NP_003049.2:p.Ser270=
ENST00000366953.8:c.808T=
MANE Select
ENSP00000355920.3:p.Ser270=
NM_003058.3:c.808T=
NP_003049.2:p.Ser270=
ENST00000366952.1:c.745T=
ENSP00000355919.1:p.Ser249=
ENST00000366953.7:c.808T=
ENSP00000355920.3:p.Ser270=
ENST00000491092.1:n.705T=
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