Canonical Allele Identifier: CA2638975884
Gene: MPO HGNC NCBI

Linked Data

gnomAD v4: 17-58280924-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280924C>T , CM000679.2:g.58280924C>T GRCh38
NC_000017.10:g.56358285C>T , CM000679.1:g.56358285C>T GRCh37
NC_000017.9:g.53713284C>T NCBI36
NG_009629.1:g.5012G>A , LRG_84:g.5012G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-166G>A MANE Select ENSP00000225275.3:n.-166G>A
ENST00000225275.3:c.-166G>A ENSP00000225275.3:n.-166G>A
NM_000250.1:c.-166G>A , LRG_84t1:c.-166G>A NP_000241.1:n.-166G>A
XM_011524821.1:c.215+1G>A XP_011523123.1:n.215+1G>A
XM_011524823.1:c.215+1G>A XP_011523125.1:n.215+1G>A
NM_000250.2:c.-166G>A MANE Select NP_000241.1:n.-166G>A
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