Canonical Allele Identifier: CA563587189
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1291996579
gnomAD v2: 5-150240586-A-T
gnomAD v3: 5-150861024-A-T
gnomAD v4: 5-150861024-A-T
MyVariant Identifiers: chr5:g.150240586A>T (hg19) chr5:g.150861024A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150861024A>T , CM000667.2:g.150861024A>T GRCh38
NC_000005.9:g.150240586A>T , CM000667.1:g.150240586A>T GRCh37
NC_000005.8:g.150220779A>T NCBI36
NG_027809.2:g.19502A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+12370A>T
XM_011537641.1:c.531+12370A>T XP_011535943.1:n.531+12370A>T
NM_001346557.1:c.531+12370A>T NP_001333486.1:n.531+12370A>T
NM_001346557.2:c.531+12370A>T NP_001333486.1:n.531+12370A>T
NR_170598.1:n.1646+12370A>T
Search 100 bp 5'
Search 100 bp 3'