Canonical Allele Identifier: CA151166211
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs3127573
gnomAD v2: 6-160681393-A-G
gnomAD v3: 6-160260361-A-G
gnomAD v4: 6-160260361-A-G
MyVariant Identifiers: chr6:g.160681393A>G (hg19) chr6:g.160260361A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160260361A>G , CM000668.2:g.160260361A>G GRCh38
NC_000006.11:g.160681393A>G , CM000668.1:g.160681393A>G GRCh37
NC_000006.10:g.160601383A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366952.1:c.-970T>C ENSP00000355919.1:n.-970T>C
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