Canonical Allele Identifier: CA805659401
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1383220217
gnomAD v3: 5-150859689-T-C
gnomAD v4: 5-150859689-T-C
MyVariant Identifiers: chr5:g.150239251T>C (hg19) chr5:g.150859689T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150859689T>C , CM000667.2:g.150859689T>C GRCh38
NC_000005.9:g.150239251T>C , CM000667.1:g.150239251T>C GRCh37
NC_000005.8:g.150219444T>C NCBI36
NG_027809.2:g.18167T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+11035T>C
XM_011537641.1:c.531+11035T>C XP_011535943.1:n.531+11035T>C
NM_001346557.1:c.531+11035T>C NP_001333486.1:n.531+11035T>C
NM_001346557.2:c.531+11035T>C NP_001333486.1:n.531+11035T>C
NR_170598.1:n.1646+11035T>C
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