Canonical Allele Identifier: CA447412318
Gene: IRGM HGNC NCBI

Linked Data

gnomAD v4: 5-150848363-T-C
MyVariant Identifiers: chr5:g.150227925T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150848363T>C , CM000667.2:g.150848363T>C GRCh38
NC_000005.9:g.150227925T>C , CM000667.1:g.150227925T>C GRCh37
NC_000005.8:g.150208118T>C NCBI36
NG_027809.1:g.6841T>C
NG_027809.2:g.6841T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000522154.2:c.240T>C MANE Select ENSP00000428220.1:p.Ser80=
ENST00000522154.1:c.240T>C ENSP00000428220.1:p.Ser80=
NM_001145805.1:c.240T>C NP_001139277.1:p.Ser80=
XM_011537641.1:c.240T>C XP_011535943.1:p.Ser80=
NM_001346557.1:c.240T>C NP_001333486.1:p.Ser80=
NM_001346557.2:c.240T>C NP_001333486.1:p.Ser80=
NM_001145805.2:c.240T>C MANE Select NP_001139277.1:p.Ser80=
NR_170598.1:n.1355T>C
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