Canonical Allele Identifier: CA15441677
Gene: SLC22A1 HGNC NCBI
COSMIC:
COSN14935616 (not active)
MyVariant.info:
GRCh38 chr6:g.160160342A>G
GRCh37 chr6:g.160581374A>G
gnomAD v2:
6:160581374 A / G
gnomAD v3:
6:160160342 A / G
gnomAD v4:
chr6-160160342-A-G
Joint Max Group AF 0.74142443 (AFR)
Genomes Max Group AF 0.74142443 (AFR)
dbSNP:
651164
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160160342A>G , CM000668.2:g.160160342A>G GRCh38
NC_000006.11:g.160581374A>G , CM000668.1:g.160581374A>G GRCh37
NC_000006.10:g.160501364A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005267102.5:c.*1492A>G XP_005267159.1:n.*1492A>G
XM_005267104.5:c.*1492A>G XP_005267161.1:n.*1492A>G
XM_005267105.5:c.*1492A>G XP_005267162.1:n.*1492A>G
XM_011536074.3:c.*1492A>G XP_011534376.1:n.*1492A>G
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