Canonical Allele Identifier: CA773481973

Gene: MPO

Linked Data

• dbSNP Id: rs1218830415
• MyVariant Identifiers: chr17:g.56351066A>G (hg19) ; chr17:g.58273705A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273705A>G , CM000679.2:g.58273705A>G	GRCh38
NC_000017.10:g.56351066A>G , CM000679.1:g.56351066A>G	GRCh37
NC_000017.9:g.53706065A>G	NCBI36
NG_009629.1:g.12231T>C , LRG_84:g.12231T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.699-36T>C
ENST00000699291.1:c.491-36T>C	ENSP00000514272.1:n.491-36T>C
ENST00000699292.1:n.370T>C
ENST00000225275.4:c.1366-36T>C MANE Select	ENSP00000225275.3:n.1366-36T>C
ENST00000225275.3:c.1366-36T>C	ENSP00000225275.3:n.1366-36T>C
NM_000250.1:c.1366-36T>C , LRG_84t1:c.1366-36T>C	NP_000241.1:n.1366-36T>C
XM_011524821.1:c.1552-36T>C	XP_011523123.1:n.1552-36T>C
XM_011524822.1:c.1081-36T>C	XP_011523124.1:n.1081-36T>C
XM_011524823.1:c.1391-36T>C	XP_011523125.1:n.1391-36T>C
NM_000250.2:c.1366-36T>C MANE Select	NP_000241.1:n.1366-36T>C