Canonical Allele Identifier: CA292020129
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs998866505
gnomAD v3: 17-58280929-T-C
gnomAD v4: 17-58280929-T-C
MyVariant Identifiers: chr17:g.56358290T>C (hg19) chr17:g.58280929T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280929T>C , CM000679.2:g.58280929T>C GRCh38
NC_000017.10:g.56358290T>C , CM000679.1:g.56358290T>C GRCh37
NC_000017.9:g.53713289T>C NCBI36
NG_009629.1:g.5007A>G , LRG_84:g.5007A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-171A>G MANE Select ENSP00000225275.3:n.-171A>G
ENST00000225275.3:c.-171A>G ENSP00000225275.3:n.-171A>G
NM_000250.1:c.-171A>G , LRG_84t1:c.-171A>G NP_000241.1:n.-171A>G
XM_011524821.1:c.211A>G XP_011523123.1:p.Ile71Val
XM_011524823.1:c.211A>G XP_011523125.1:p.Ile71Val
NM_000250.2:c.-171A>G MANE Select NP_000241.1:n.-171A>G
Search 100 bp 5'
Search 100 bp 3'