Canonical Allele Identifier: CA2638975857
Gene: MPO HGNC NCBI

Linked Data

gnomAD v4: 17-58280902-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280902A>G , CM000679.2:g.58280902A>G GRCh38
NC_000017.10:g.56358263A>G , CM000679.1:g.56358263A>G GRCh37
NC_000017.9:g.53713262A>G NCBI36
NG_009629.1:g.5034T>C , LRG_84:g.5034T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-144T>C MANE Select ENSP00000225275.3:n.-144T>C
ENST00000225275.3:c.-144T>C ENSP00000225275.3:n.-144T>C
NM_000250.1:c.-144T>C , LRG_84t1:c.-144T>C NP_000241.1:n.-144T>C
XM_011524821.1:c.215+23T>C XP_011523123.1:n.215+23T>C
XM_011524823.1:c.215+23T>C XP_011523125.1:n.215+23T>C
NM_000250.2:c.-144T>C MANE Select NP_000241.1:n.-144T>C
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