Canonical Allele Identifier: CA129183277
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1053318510
gnomAD v2: 5-150240591-C-G
gnomAD v3: 5-150861029-C-G
gnomAD v4: 5-150861029-C-G
MyVariant Identifiers: chr5:g.150240591C>G (hg19) chr5:g.150861029C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150861029C>G , CM000667.2:g.150861029C>G GRCh38
NC_000005.9:g.150240591C>G , CM000667.1:g.150240591C>G GRCh37
NC_000005.8:g.150220784C>G NCBI36
NG_027809.2:g.19507C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+12375C>G
XM_011537641.1:c.531+12375C>G XP_011535943.1:n.531+12375C>G
NM_001346557.1:c.531+12375C>G NP_001333486.1:n.531+12375C>G
NM_001346557.2:c.531+12375C>G NP_001333486.1:n.531+12375C>G
NR_170598.1:n.1646+12375C>G
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