Canonical Allele Identifier: CA2638975883
Gene: MPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280923A>C , CM000679.2:g.58280923A>C GRCh38
NC_000017.10:g.56358284A>C , CM000679.1:g.56358284A>C GRCh37
NC_000017.9:g.53713283A>C NCBI36
NG_009629.1:g.5013T>G , LRG_84:g.5013T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-165T>G MANE Select ENSP00000225275.3:n.-165T>G
ENST00000225275.3:c.-165T>G ENSP00000225275.3:n.-165T>G
NM_000250.1:c.-165T>G , LRG_84t1:c.-165T>G NP_000241.1:n.-165T>G
XM_011524821.1:c.215+2T>G XP_011523123.1:n.215+2T>G
XM_011524823.1:c.215+2T>G XP_011523125.1:n.215+2T>G
NM_000250.2:c.-165T>G MANE Select NP_000241.1:n.-165T>G