Canonical Allele Identifier: CA447412308
Gene: IRGM HGNC NCBI

Linked Data

gnomAD v4: 5-150848351-C-A
MyVariant Identifiers: chr5:g.150227913C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150848351C>A , CM000667.2:g.150848351C>A GRCh38
NC_000005.9:g.150227913C>A , CM000667.1:g.150227913C>A GRCh37
NC_000005.8:g.150208106C>A NCBI36
NG_027809.1:g.6829C>A
NG_027809.2:g.6829C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000522154.2:c.228C>A MANE Select ENSP00000428220.1:p.Ala76=
ENST00000522154.1:c.228C>A ENSP00000428220.1:p.Ala76=
NM_001145805.1:c.228C>A NP_001139277.1:p.Ala76=
XM_011537641.1:c.228C>A XP_011535943.1:p.Ala76=
NM_001346557.1:c.228C>A NP_001333486.1:p.Ala76=
NM_001346557.2:c.228C>A NP_001333486.1:p.Ala76=
NM_001145805.2:c.228C>A MANE Select NP_001139277.1:p.Ala76=
NR_170598.1:n.1343C>A
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