Canonical Allele Identifier: CA2638974946

Gene: MPO

Linked Data

• dbSNP Id: rs2143983146
• gnomAD v4: 17-58280292-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58280292T>C , CM000679.2:g.58280292T>C	GRCh38
NC_000017.10:g.56357653T>C , CM000679.1:g.56357653T>C	GRCh37
NC_000017.9:g.53712652T>C	NCBI36
NG_009629.1:g.5644A>G , LRG_84:g.5644A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000225275.4:c.248+74A>G MANE Select	ENSP00000225275.3:n.248+74A>G
ENST00000225275.3:c.248+74A>G	ENSP00000225275.3:n.248+74A>G
ENST00000580005.1:n.251A>G
NM_000250.1:c.248+74A>G , LRG_84t1:c.248+74A>G	NP_000241.1:n.248+74A>G
XM_011524821.1:c.434+74A>G	XP_011523123.1:n.434+74A>G
XM_011524822.1:c.-37-278A>G	XP_011523124.1:n.-37-278A>G
XM_011524823.1:c.434+74A>G	XP_011523125.1:n.434+74A>G
NM_000250.2:c.248+74A>G MANE Select	NP_000241.1:n.248+74A>G