Canonical Allele Identifier: CA2267633996
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1163102880

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58279464G>A , CM000679.2:g.58279464G>A GRCh38
NC_000017.10:g.56356825G>A , CM000679.1:g.56356825G>A GRCh37
NC_000017.9:g.53711824G>A NCBI36
NG_009629.1:g.6472C>T , LRG_84:g.6472C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.549-38C>T MANE Select ENSP00000225275.3:n.549-38C>T
ENST00000225275.3:c.549-38C>T ENSP00000225275.3:n.549-38C>T
NM_000250.1:c.549-38C>T , LRG_84t1:c.549-38C>T NP_000241.1:n.549-38C>T
XM_011524821.1:c.735-38C>T XP_011523123.1:n.735-38C>T
XM_011524822.1:c.264-38C>T XP_011523124.1:n.264-38C>T
XM_011524823.1:c.735-38C>T XP_011523125.1:n.735-38C>T
NM_000250.2:c.549-38C>T MANE Select NP_000241.1:n.549-38C>T