Canonical Allele Identifier: CA1082927627
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs186376772
gnomAD v3: 5-150859776-C-A
gnomAD v4: 5-150859776-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150859776C>A , CM000667.2:g.150859776C>A GRCh38
NC_000005.9:g.150239338C>A , CM000667.1:g.150239338C>A GRCh37
NC_000005.8:g.150219531C>A NCBI36
NG_027809.2:g.18254C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+11122C>A
XM_011537641.1:c.531+11122C>A XP_011535943.1:n.531+11122C>A
NM_001346557.1:c.531+11122C>A NP_001333486.1:n.531+11122C>A
NM_001346557.2:c.531+11122C>A NP_001333486.1:n.531+11122C>A
NR_170598.1:n.1646+11122C>A
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