Canonical Allele Identifier: CA1676979838
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs1440673215
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260402C>A , CM000668.2:g.160260402C>A GRCh38
NC_000006.11:g.160681434C>A , CM000668.1:g.160681434C>A GRCh37
NC_000006.10:g.160601424C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366952.1:c.-1011G>T ENSP00000355919.1:n.-1011G>T
Search 100 bp 5'
Search 100 bp 3'