Canonical Allele Identifier: CA453014102
Gene: SLC22A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.160668297G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160247265G>T , CM000668.2:g.160247265G>T GRCh38
NC_000006.11:g.160668297G>T , CM000668.1:g.160668297G>T GRCh37
NC_000006.10:g.160588287G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.876C>A MANE Select ENSP00000355920.3:p.Ser292=
ENST00000366952.1:c.813C>A ENSP00000355919.1:p.Ser271=
ENST00000366953.7:c.876C>A ENSP00000355920.3:p.Ser292=
ENST00000491092.1:n.773C>A
NM_003058.3:c.876C>A NP_003049.2:p.Ser292=
NM_003058.4:c.876C>A MANE Select NP_003049.2:p.Ser292=
Search 100 bp 5'
Search 100 bp 3'