Canonical Allele Identifier: CA129182658
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs931614323
gnomAD v3: 5-150859797-A-G
gnomAD v4: 5-150859797-A-G
MyVariant Identifiers: chr5:g.150239359A>G (hg19) chr5:g.150859797A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150859797A>G , CM000667.2:g.150859797A>G GRCh38
NC_000005.9:g.150239359A>G , CM000667.1:g.150239359A>G GRCh37
NC_000005.8:g.150219552A>G NCBI36
NG_027809.2:g.18275A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+11143A>G
XM_011537641.1:c.531+11143A>G XP_011535943.1:n.531+11143A>G
NM_001346557.1:c.531+11143A>G NP_001333486.1:n.531+11143A>G
NM_001346557.2:c.531+11143A>G NP_001333486.1:n.531+11143A>G
NR_170598.1:n.1646+11143A>G
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