Canonical Allele Identifier: CA1676974871
Community Standard Title: NM_003058.4(SLC22A2):c.808T= (p.Ser270=)
Gene: SLC22A2 HGNC NCBI

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=