Canonical Allele Identifier: CA292020105
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs971157099
gnomAD v4: 17-58280910-A-G
MyVariant Identifiers: chr17:g.56358271A>G (hg19) chr17:g.58280910A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280910A>G , CM000679.2:g.58280910A>G GRCh38
NC_000017.10:g.56358271A>G , CM000679.1:g.56358271A>G GRCh37
NC_000017.9:g.53713270A>G NCBI36
NG_009629.1:g.5026T>C , LRG_84:g.5026T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-152T>C MANE Select ENSP00000225275.3:n.-152T>C
ENST00000225275.3:c.-152T>C ENSP00000225275.3:n.-152T>C
NM_000250.1:c.-152T>C , LRG_84t1:c.-152T>C NP_000241.1:n.-152T>C
XM_011524821.1:c.215+15T>C XP_011523123.1:n.215+15T>C
XM_011524823.1:c.215+15T>C XP_011523125.1:n.215+15T>C
NM_000250.2:c.-152T>C MANE Select NP_000241.1:n.-152T>C
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