Canonical Allele Identifier: CA3650097

Gene: TPMT

Linked Data

• dbSNP Id: rs781193166
• ExAC: 6:18131032 A / G
• gnomAD v2: 6-18131032-A-G
• gnomAD v3: 6-18130801-A-G
• gnomAD v4: 6-18130801-A-G
• MyVariant Identifiers: chr6:g.18131032A>G (hg19) ; chr6:g.18130801A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130801A>G , CM000668.2:g.18130801A>G	GRCh38
NC_000006.11:g.18131032A>G , CM000668.1:g.18131032A>G	GRCh37
NC_000006.10:g.18239011A>G	NCBI36
NG_012137.2:g.29343T>C
NG_012137.3:g.29343T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.626-21T>C MANE Select	ENSP00000312304.4:n.626-21T>C
ENST00000309983.4:c.626-21T>C	ENSP00000312304.4:n.626-21T>C
NM_000367.3:c.626-21T>C	NP_000358.1:n.626-21T>C
XM_011514839.1:c.581-21T>C	XP_011513141.1:n.581-21T>C
XM_011514840.1:c.557-21T>C	XP_011513142.1:n.557-21T>C
NM_000367.4:c.626-21T>C	NP_000358.1:n.626-21T>C
NM_001346817.1:c.626-21T>C	NP_001333746.1:n.626-21T>C
NM_001346818.1:c.581-21T>C	NP_001333747.1:n.581-21T>C
NM_000367.5:c.626-21T>C MANE Select	NP_000358.1:n.626-21T>C