Canonical Allele Identifier: CA1591137765
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1754120114

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860439C>G , CM000667.2:g.150860439C>G GRCh38
NC_000005.9:g.150240001C>G , CM000667.1:g.150240001C>G GRCh37
NC_000005.8:g.150220194C>G NCBI36
NG_027809.2:g.18917C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11785C>G
XM_011537641.1:c.531+11785C>G XP_011535943.1:n.531+11785C>G
NM_001346557.1:c.531+11785C>G NP_001333486.1:n.531+11785C>G
NM_001346557.2:c.531+11785C>G NP_001333486.1:n.531+11785C>G
NR_170598.1:n.1646+11785C>G