Canonical Allele Identifier: CA151166247
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs903135559
gnomAD v2: 6-160681418-C-T
gnomAD v3: 6-160260386-C-T
gnomAD v4: 6-160260386-C-T
MyVariant Identifiers: chr6:g.160681418C>T (hg19) chr6:g.160260386C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260386C>T , CM000668.2:g.160260386C>T GRCh38
NC_000006.11:g.160681418C>T , CM000668.1:g.160681418C>T GRCh37
NC_000006.10:g.160601408C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366952.1:c.-995G>A ENSP00000355919.1:n.-995G>A
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