Canonical Allele Identifier: CA822681093
Gene: TPMT HGNC NCBI

Linked Data

dbSNP Id: rs1386683387
MyVariant Identifiers: chr6:g.18144044T>G (hg19) chr6:g.18143813T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18143813T>G , CM000668.2:g.18143813T>G GRCh38
NC_000006.11:g.18144044T>G , CM000668.1:g.18144044T>G GRCh37
NC_000006.10:g.18252023T>G NCBI36
NG_012137.2:g.16331A>C
NG_012137.3:g.16331A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.234-85A>C MANE Select ENSP00000312304.4:n.234-85A>C
ENST00000309983.4:c.234-85A>C ENSP00000312304.4:n.234-85A>C
NM_000367.3:c.234-85A>C NP_000358.1:n.234-85A>C
XM_011514839.1:c.234-85A>C XP_011513141.1:n.234-85A>C
XM_011514840.1:c.165-85A>C XP_011513142.1:n.165-85A>C
NM_000367.4:c.234-85A>C NP_000358.1:n.234-85A>C
NM_001346817.1:c.234-85A>C NP_001333746.1:n.234-85A>C
NM_001346818.1:c.234-85A>C NP_001333747.1:n.234-85A>C
NM_000367.5:c.234-85A>C MANE Select NP_000358.1:n.234-85A>C
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