Canonical Allele Identifier: CA2638975861
Gene: MPO HGNC NCBI

Linked Data

gnomAD v4: 17-58280904-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280904G>C , CM000679.2:g.58280904G>C GRCh38
NC_000017.10:g.56358265G>C , CM000679.1:g.56358265G>C GRCh37
NC_000017.9:g.53713264G>C NCBI36
NG_009629.1:g.5032C>G , LRG_84:g.5032C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-146C>G MANE Select ENSP00000225275.3:n.-146C>G
ENST00000225275.3:c.-146C>G ENSP00000225275.3:n.-146C>G
NM_000250.1:c.-146C>G , LRG_84t1:c.-146C>G NP_000241.1:n.-146C>G
XM_011524821.1:c.215+21C>G XP_011523123.1:n.215+21C>G
XM_011524823.1:c.215+21C>G XP_011523125.1:n.215+21C>G
NM_000250.2:c.-146C>G MANE Select NP_000241.1:n.-146C>G
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