Canonical Allele Identifier: CA361785101

Gene: IRGM

Linked Data

• gnomAD v4: 5-150848263-C-T
• MyVariant Identifiers: chr5:g.150227825C>T (hg19) ; chr5:g.150848263C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150848263C>T , CM000667.2:g.150848263C>T	GRCh38
NC_000005.9:g.150227825C>T , CM000667.1:g.150227825C>T	GRCh37
NC_000005.8:g.150208018C>T	NCBI36
NG_027809.1:g.6741C>T
NG_027809.2:g.6741C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000522154.2:c.140C>T MANE Select	ENSP00000428220.1:p.Ser47Phe
ENST00000522154.1:c.140C>T	ENSP00000428220.1:p.Ser47Phe
NM_001145805.1:c.140C>T	NP_001139277.1:p.Ser47Phe
XM_011537641.1:c.140C>T	XP_011535943.1:p.Ser47Phe
NM_001346557.1:c.140C>T	NP_001333486.1:p.Ser47Phe
NM_001346557.2:c.140C>T	NP_001333486.1:p.Ser47Phe
NM_001145805.2:c.140C>T MANE Select	NP_001139277.1:p.Ser47Phe
NR_170598.1:n.1255C>T