Canonical Allele Identifier: CA2681069917
Gene: SLC22A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249157G>C , CM000668.2:g.160249157G>C GRCh38
NC_000006.11:g.160670189G>C , CM000668.1:g.160670189G>C GRCh37
NC_000006.10:g.160590179G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+59C>G MANE Select ENSP00000355920.3:n.842+59C>G
ENST00000366952.1:c.779+59C>G ENSP00000355919.1:n.779+59C>G
ENST00000366953.7:c.842+59C>G ENSP00000355920.3:n.842+59C>G
ENST00000491092.1:n.739+59C>G
NM_003058.3:c.842+59C>G NP_003049.2:n.842+59C>G
NM_003058.4:c.842+59C>G MANE Select NP_003049.2:n.842+59C>G