Canonical Allele Identifier: CA129183100
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs997367636
MyVariant Identifiers: chr5:g.150240258T>A (hg19) chr5:g.150860696T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860696T>A , CM000667.2:g.150860696T>A GRCh38
NC_000005.9:g.150240258T>A , CM000667.1:g.150240258T>A GRCh37
NC_000005.8:g.150220451T>A NCBI36
NG_027809.2:g.19174T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+12042T>A
XM_011537641.1:c.531+12042T>A XP_011535943.1:n.531+12042T>A
NM_001346557.1:c.531+12042T>A NP_001333486.1:n.531+12042T>A
NM_001346557.2:c.531+12042T>A NP_001333486.1:n.531+12042T>A
NR_170598.1:n.1646+12042T>A
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