Canonical Allele Identifier: CA134961583
Gene: TPMT HGNC NCBI

Linked Data

dbSNP Id: rs985128045
MyVariant Identifiers: chr6:g.18131110C>T (hg19) chr6:g.18130879C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130879C>T , CM000668.2:g.18130879C>T GRCh38
NC_000006.11:g.18131110C>T , CM000668.1:g.18131110C>T GRCh37
NC_000006.10:g.18239089C>T NCBI36
NG_012137.2:g.29265G>A
NG_012137.3:g.29265G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.626-99G>A MANE Select ENSP00000312304.4:n.626-99G>A
ENST00000309983.4:c.626-99G>A ENSP00000312304.4:n.626-99G>A
NM_000367.3:c.626-99G>A NP_000358.1:n.626-99G>A
XM_011514839.1:c.581-99G>A XP_011513141.1:n.581-99G>A
XM_011514840.1:c.557-99G>A XP_011513142.1:n.557-99G>A
NM_000367.4:c.626-99G>A NP_000358.1:n.626-99G>A
NM_001346817.1:c.626-99G>A NP_001333746.1:n.626-99G>A
NM_001346818.1:c.581-99G>A NP_001333747.1:n.581-99G>A
NM_000367.5:c.626-99G>A MANE Select NP_000358.1:n.626-99G>A
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