Canonical Allele Identifier: CA129183019
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1031904533

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860518G>C , CM000667.2:g.150860518G>C GRCh38
NC_000005.9:g.150240080G>C , CM000667.1:g.150240080G>C GRCh37
NC_000005.8:g.150220273G>C NCBI36
NG_027809.2:g.18996G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11864G>C
XM_011537641.1:c.531+11864G>C XP_011535943.1:n.531+11864G>C
NM_001346557.1:c.531+11864G>C NP_001333486.1:n.531+11864G>C
NM_001346557.2:c.531+11864G>C NP_001333486.1:n.531+11864G>C
NR_170598.1:n.1646+11864G>C