Canonical Allele Identifier: CA773487793
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1491253260
MyVariant Identifiers: chr17:g.56358482_56358483insTTTTA (hg19) chr17:g.58281121_58281122insTTTTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281125_58281126insATTTT , CM000679.2:g.58281125_58281126insATTTT GRCh38
NC_000017.10:g.56358486_56358487insATTTT , CM000679.1:g.56358486_56358487insATTTT GRCh37
NC_000017.9:g.53713485_53713486insATTTT NCBI36
NG_009629.1:g.4814_4815insTAAAA , LRG_84:g.4814_4815insTAAAA

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.71-53_71-52insTAAAA XP_011523123.1:n.71-53_71-52insTAAAA
XM_011524823.1:c.71-53_71-52insTAAAA XP_011523125.1:n.71-53_71-52insTAAAA
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