Canonical Allele Identifier: CA1676974790
Gene: SLC22A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249075T= , CM000668.2:g.160249075T= GRCh38
NC_000006.11:g.160670107T= , CM000668.1:g.160670107T= GRCh37
NC_000006.10:g.160590097T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+141A= MANE Select ENSP00000355920.3:n.842+141A=
ENST00000366952.1:c.779+141A= ENSP00000355919.1:n.779+141A=
ENST00000366953.7:c.842+141A= ENSP00000355920.3:n.842+141A=
ENST00000491092.1:n.739+141A=
NM_003058.3:c.842+141A= NP_003049.2:n.842+141A=
NM_003058.4:c.842+141A= MANE Select NP_003049.2:n.842+141A=
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