Canonical Allele Identifier: CA12417982
Gene: SLC22A2 HGNC NCBI

Linked Data

dbSNP Id: rs316006
gnomAD v2: 6-160646365-T-A
gnomAD v3: 6-160225333-T-A
gnomAD v4: 6-160225333-T-A
MyVariant Identifiers: chr6:g.160646365T>A (hg19) chr6:g.160225333T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160225333T>A , CM000668.2:g.160225333T>A GRCh38
NC_000006.11:g.160646365T>A , CM000668.1:g.160646365T>A GRCh37
NC_000006.10:g.160566355T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.1502-529A>T MANE Select ENSP00000355920.3:n.1502-529A>T
ENST00000366953.7:c.1502-529A>T ENSP00000355920.3:n.1502-529A>T
ENST00000486916.5:n.541-529A>T
ENST00000491092.1:n.1399-529A>T
NM_003058.3:c.1502-529A>T NP_003049.2:n.1502-529A>T
NM_003058.4:c.1502-529A>T MANE Select NP_003049.2:n.1502-529A>T
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