Canonical Allele Identifier: CA1086467191
Gene: TPMT HGNC NCBI

Linked Data

dbSNP Id: rs1783921774
gnomAD v3: 6-18130561-G-C
gnomAD v4: 6-18130561-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130561G>C , CM000668.2:g.18130561G>C GRCh38
NC_000006.11:g.18130792G>C , CM000668.1:g.18130792G>C GRCh37
NC_000006.10:g.18238771G>C NCBI36
NG_012137.2:g.29583C>G
NG_012137.3:g.29583C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.*107C>G MANE Select ENSP00000312304.4:n.*107C>G
ENST00000309983.4:c.*107C>G ENSP00000312304.4:n.*107C>G
NM_000367.3:c.*107C>G NP_000358.1:n.*107C>G
XM_011514839.1:c.*107C>G XP_011513141.1:n.*107C>G
XM_011514840.1:c.*107C>G XP_011513142.1:n.*107C>G
NM_000367.4:c.*107C>G NP_000358.1:n.*107C>G
NM_001346817.1:c.*107C>G NP_001333746.1:n.*107C>G
NM_001346818.1:c.*107C>G NP_001333747.1:n.*107C>G
NM_000367.5:c.*107C>G MANE Select NP_000358.1:n.*107C>G