Canonical Allele Identifier: CA1676974828
Gene: SLC22A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249165A= , CM000668.2:g.160249165A= GRCh38
NC_000006.11:g.160670197A= , CM000668.1:g.160670197A= GRCh37
NC_000006.10:g.160590187A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+51T= MANE Select ENSP00000355920.3:n.842+51T=
ENST00000366952.1:c.779+51T= ENSP00000355919.1:n.779+51T=
ENST00000366953.7:c.842+51T= ENSP00000355920.3:n.842+51T=
ENST00000491092.1:n.739+51T=
NM_003058.3:c.842+51T= NP_003049.2:n.842+51T=
NM_003058.4:c.842+51T= MANE Select NP_003049.2:n.842+51T=