Canonical Allele Identifier: CA822712281
Gene: TPMT HGNC NCBI

Linked Data

dbSNP Id: rs1259065104

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130629A>G , CM000668.2:g.18130629A>G GRCh38
NC_000006.11:g.18130860A>G , CM000668.1:g.18130860A>G GRCh37
NC_000006.10:g.18238839A>G NCBI36
NG_012137.2:g.29515T>C
NG_012137.3:g.29515T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.*39T>C MANE Select ENSP00000312304.4:n.*39T>C
ENST00000309983.4:c.*39T>C ENSP00000312304.4:n.*39T>C
NM_000367.3:c.*39T>C NP_000358.1:n.*39T>C
XM_011514839.1:c.*39T>C XP_011513141.1:n.*39T>C
XM_011514840.1:c.*39T>C XP_011513142.1:n.*39T>C
NM_000367.4:c.*39T>C NP_000358.1:n.*39T>C
NM_001346817.1:c.*39T>C NP_001333746.1:n.*39T>C
NM_001346818.1:c.*39T>C NP_001333747.1:n.*39T>C
NM_000367.5:c.*39T>C MANE Select NP_000358.1:n.*39T>C