Canonical Allele Identifier: CA151166211
Gene: SLC22A2 HGNC NCBI
COSMIC:
COSN14902953 (not active)
MyVariant.info:
GRCh38 chr6:g.160260361A>G
GRCh37 chr6:g.160681393A>G
gnomAD v2:
6:160681393 A / G
gnomAD v3:
6:160260361 A / G
gnomAD v4:
chr6-160260361-A-G
Joint Max Group AF 0.15212203 (AFR)
Genomes Max Group AF 0.15212203 (AFR)
dbSNP:
3127573
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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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