Canonical Allele Identifier: CA2638975870
Gene: MPO HGNC NCBI

Linked Data

gnomAD v4: 17-58280913-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280913T>C , CM000679.2:g.58280913T>C GRCh38
NC_000017.10:g.56358274T>C , CM000679.1:g.56358274T>C GRCh37
NC_000017.9:g.53713273T>C NCBI36
NG_009629.1:g.5023A>G , LRG_84:g.5023A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-155A>G MANE Select ENSP00000225275.3:n.-155A>G
ENST00000225275.3:c.-155A>G ENSP00000225275.3:n.-155A>G
NM_000250.1:c.-155A>G , LRG_84t1:c.-155A>G NP_000241.1:n.-155A>G
XM_011524821.1:c.215+12A>G XP_011523123.1:n.215+12A>G
XM_011524823.1:c.215+12A>G XP_011523125.1:n.215+12A>G
NM_000250.2:c.-155A>G MANE Select NP_000241.1:n.-155A>G
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