Canonical Allele Identifier: CA1591137886
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs910117874
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860708A>T , CM000667.2:g.150860708A>T GRCh38
NC_000005.9:g.150240270A>T , CM000667.1:g.150240270A>T GRCh37
NC_000005.8:g.150220463A>T NCBI36
NG_027809.2:g.19186A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+12054A>T
XM_011537641.1:c.531+12054A>T XP_011535943.1:n.531+12054A>T
NM_001346557.1:c.531+12054A>T NP_001333486.1:n.531+12054A>T
NM_001346557.2:c.531+12054A>T NP_001333486.1:n.531+12054A>T
NR_170598.1:n.1646+12054A>T
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