Canonical Allele Identifier: CA2267634853
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1598044167
gnomAD v4: 17-58280926-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280926T>G , CM000679.2:g.58280926T>G GRCh38
NC_000017.10:g.56358287T>G , CM000679.1:g.56358287T>G GRCh37
NC_000017.9:g.53713286T>G NCBI36
NG_009629.1:g.5010A>C , LRG_84:g.5010A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-168A>C MANE Select ENSP00000225275.3:n.-168A>C
ENST00000225275.3:c.-168A>C ENSP00000225275.3:n.-168A>C
NM_000250.1:c.-168A>C , LRG_84t1:c.-168A>C NP_000241.1:n.-168A>C
XM_011524821.1:c.214A>C XP_011523123.1:p.Arg72=
XM_011524823.1:c.214A>C XP_011523125.1:p.Arg72=
NM_000250.2:c.-168A>C MANE Select NP_000241.1:n.-168A>C
Search 100 bp 5'
Search 100 bp 3'