Canonical Allele Identifier: CA361785293
Gene: IRGM HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.150227921T>A (hg19) chr5:g.150848359T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150848359T>A , CM000667.2:g.150848359T>A GRCh38
NC_000005.9:g.150227921T>A , CM000667.1:g.150227921T>A GRCh37
NC_000005.8:g.150208114T>A NCBI36
NG_027809.1:g.6837T>A
NG_027809.2:g.6837T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000522154.2:c.236T>A MANE Select ENSP00000428220.1:p.Phe79Tyr
ENST00000522154.1:c.236T>A ENSP00000428220.1:p.Phe79Tyr
NM_001145805.1:c.236T>A NP_001139277.1:p.Phe79Tyr
XM_011537641.1:c.236T>A XP_011535943.1:p.Phe79Tyr
NM_001346557.1:c.236T>A NP_001333486.1:p.Phe79Tyr
NM_001346557.2:c.236T>A NP_001333486.1:p.Phe79Tyr
NM_001145805.2:c.236T>A MANE Select NP_001139277.1:p.Phe79Tyr
NR_170598.1:n.1351T>A
Search 100 bp 5'
Search 100 bp 3'