Canonical Allele Identifier: CA805659476
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1450139470
gnomAD v3: 5-150859863-C-T
gnomAD v4: 5-150859863-C-T
MyVariant Identifiers: chr5:g.150239425C>T (hg19) chr5:g.150859863C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150859863C>T , CM000667.2:g.150859863C>T GRCh38
NC_000005.9:g.150239425C>T , CM000667.1:g.150239425C>T GRCh37
NC_000005.8:g.150219618C>T NCBI36
NG_027809.2:g.18341C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+11209C>T
XM_011537641.1:c.531+11209C>T XP_011535943.1:n.531+11209C>T
NM_001346557.1:c.531+11209C>T NP_001333486.1:n.531+11209C>T
NM_001346557.2:c.531+11209C>T NP_001333486.1:n.531+11209C>T
NR_170598.1:n.1646+11209C>T
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