Canonical Allele Identifier: CA571906250

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1376098861
• gnomAD v2: 6-160857906-CTTGGTAA-C
• gnomAD v4: 6-160436874-CTTGGTAA-C
• MyVariant Identifiers: chr6:g.160857907_160857913del (hg19) ; chr6:g.160436875_160436881del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436875_160436881del , CM000668.2:g.160436875_160436881del	GRCh38
NC_000006.11:g.160857907_160857913del , CM000668.1:g.160857907_160857913del	GRCh37
NC_000006.10:g.160777897_160777903del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1071_1073+4del
ENST00000275300.2:c.1071_1073+4del
NM_021977.3:c.1071_1073+4del
XM_005267106.3:c.678_680+4del
XM_011536075.1:c.615_617+4del
XM_011536076.1:c.615_617+4del
XM_011536077.1:c.615_617+4del
XR_245546.1:n.1018-5886_1018-5880del
XM_005267106.5:c.678_680+4del
XM_011536075.2:c.615_617+4del
XM_011536076.3:c.615_617+4del
XM_017011203.2:c.615_617+4del
XR_001743588.1:n.1018-122_1018-116del
XR_001743589.1:n.1018-5886_1018-5880del
NM_021977.4:c.1071_1073+4del