Canonical Allele Identifier: CA480603021
Gene: PPM1H HGNC NCBI
GAPDHP44 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.63149145C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.62755365C>T , CM000674.2:g.62755365C>T GRCh38
NC_000012.11:g.63149145C>T , CM000674.1:g.63149145C>T GRCh37
NC_000012.10:g.61435412C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000228705.7:c.870-17779G>A (PPM1H) MANE Select ENSP00000228705.5:n.870-17779G>A
ENST00000228705.6:c.870-17779G>A (PPM1H) ENSP00000228705.5:n.870-17779G>A
ENST00000513513.1:n.139C>T (GAPDHP44)
ENST00000551519.1:n.260-17779G>A (PPM1H)
NM_020700.1:c.870-17779G>A (PPM1H) NP_065751.1:n.870-17779G>A
XM_011538578.1:c.756-17779G>A (PPM1H) XP_011536880.1:n.756-17779G>A
XM_011538579.1:c.117-17779G>A (PPM1H) XP_011536881.1:n.117-17779G>A
XM_011538578.2:c.756-17779G>A (PPM1H) XP_011536880.1:n.756-17779G>A
XM_017019676.2:c.870-17779G>A (PPM1H) XP_016875165.1:n.870-17779G>A
NM_020700.2:c.870-17779G>A (PPM1H) MANE Select NP_065751.1:n.870-17779G>A