Canonical Allele Identifier: CA1613558677
Gene: TPMT HGNC NCBI

Linked Data

dbSNP Id: rs1784104921
gnomAD v4: 6-18139599-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18139599T>A , CM000668.2:g.18139599T>A GRCh38
NC_000006.11:g.18139830T>A , CM000668.1:g.18139830T>A GRCh37
NC_000006.10:g.18247809T>A NCBI36
NG_012137.2:g.20545A>T
NG_012137.3:g.20545A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.419+66A>T MANE Select ENSP00000312304.4:n.419+66A>T
ENST00000309983.4:c.419+66A>T ENSP00000312304.4:n.419+66A>T
NM_000367.3:c.419+66A>T NP_000358.1:n.419+66A>T
XM_011514839.1:c.419+66A>T XP_011513141.1:n.419+66A>T
XM_011514840.1:c.350+66A>T XP_011513142.1:n.350+66A>T
NM_000367.4:c.419+66A>T NP_000358.1:n.419+66A>T
NM_001346817.1:c.419+66A>T NP_001333746.1:n.419+66A>T
NM_001346818.1:c.419+66A>T NP_001333747.1:n.419+66A>T
NM_000367.5:c.419+66A>T MANE Select NP_000358.1:n.419+66A>T