Canonical Allele Identifier: CA361785077
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1414501331
gnomAD v2: 5-150227816-A-G
gnomAD v3: 5-150848254-A-G
gnomAD v4: 5-150848254-A-G
MyVariant Identifiers: chr5:g.150227816A>G (hg19) chr5:g.150848254A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150848254A>G , CM000667.2:g.150848254A>G GRCh38
NC_000005.9:g.150227816A>G , CM000667.1:g.150227816A>G GRCh37
NC_000005.8:g.150208009A>G NCBI36
NG_027809.1:g.6732A>G
NG_027809.2:g.6732A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000522154.2:c.131A>G MANE Select ENSP00000428220.1:p.Asn44Ser
ENST00000522154.1:c.131A>G ENSP00000428220.1:p.Asn44Ser
NM_001145805.1:c.131A>G NP_001139277.1:p.Asn44Ser
XM_011537641.1:c.131A>G XP_011535943.1:p.Asn44Ser
NM_001346557.1:c.131A>G NP_001333486.1:p.Asn44Ser
NM_001346557.2:c.131A>G NP_001333486.1:p.Asn44Ser
NM_001145805.2:c.131A>G MANE Select NP_001139277.1:p.Asn44Ser
NR_170598.1:n.1246A>G
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