Canonical Allele Identifier: CA501321981
Gene: MPO HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.56357756C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280395C>G , CM000679.2:g.58280395C>G GRCh38
NC_000017.10:g.56357756C>G , CM000679.1:g.56357756C>G GRCh37
NC_000017.9:g.53712755C>G NCBI36
NG_009629.1:g.5541G>C , LRG_84:g.5541G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.219G>C MANE Select ENSP00000225275.3:p.Val73=
ENST00000225275.3:c.219G>C ENSP00000225275.3:p.Val73=
ENST00000580005.1:n.148G>C
NM_000250.1:c.219G>C , LRG_84t1:c.219G>C NP_000241.1:p.Val73=
XM_011524821.1:c.405G>C XP_011523123.1:p.Val135=
XM_011524822.1:c.-38+210G>C XP_011523124.1:n.-38+210G>C
XM_011524823.1:c.405G>C XP_011523125.1:p.Val135=
NM_000250.2:c.219G>C MANE Select NP_000241.1:p.Val73=