Canonical Allele Identifier: CA1591137489
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1754109973
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150859762T>A , CM000667.2:g.150859762T>A GRCh38
NC_000005.9:g.150239324T>A , CM000667.1:g.150239324T>A GRCh37
NC_000005.8:g.150219517T>A NCBI36
NG_027809.2:g.18240T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+11108T>A
XM_011537641.1:c.531+11108T>A XP_011535943.1:n.531+11108T>A
NM_001346557.1:c.531+11108T>A NP_001333486.1:n.531+11108T>A
NM_001346557.2:c.531+11108T>A NP_001333486.1:n.531+11108T>A
NR_170598.1:n.1646+11108T>A
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