Canonical Allele Identifier: CA1082927735
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1754113558
gnomAD v3: 5-150860012-C-T
gnomAD v4: 5-150860012-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860012C>T , CM000667.2:g.150860012C>T GRCh38
NC_000005.9:g.150239574C>T , CM000667.1:g.150239574C>T GRCh37
NC_000005.8:g.150219767C>T NCBI36
NG_027809.2:g.18490C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+11358C>T
XM_011537641.1:c.531+11358C>T XP_011535943.1:n.531+11358C>T
NM_001346557.1:c.531+11358C>T NP_001333486.1:n.531+11358C>T
NM_001346557.2:c.531+11358C>T NP_001333486.1:n.531+11358C>T
NR_170598.1:n.1646+11358C>T
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