Canonical Allele Identifier: CA1676974797
Gene: SLC22A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249090T= , CM000668.2:g.160249090T= GRCh38
NC_000006.11:g.160670122T= , CM000668.1:g.160670122T= GRCh37
NC_000006.10:g.160590112T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366953.8:c.842+126A= MANE Select ENSP00000355920.3:n.842+126A=
ENST00000366952.1:c.779+126A= ENSP00000355919.1:n.779+126A=
ENST00000366953.7:c.842+126A= ENSP00000355920.3:n.842+126A=
ENST00000491092.1:n.739+126A=
NM_003058.3:c.842+126A= NP_003049.2:n.842+126A=
NM_003058.4:c.842+126A= MANE Select NP_003049.2:n.842+126A=