Canonical Allele Identifier: CA805659966
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1171699024

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860686G>T , CM000667.2:g.150860686G>T GRCh38
NC_000005.9:g.150240248G>T , CM000667.1:g.150240248G>T GRCh37
NC_000005.8:g.150220441G>T NCBI36
NG_027809.2:g.19164G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+12032G>T
XM_011537641.1:c.531+12032G>T XP_011535943.1:n.531+12032G>T
NM_001346557.1:c.531+12032G>T NP_001333486.1:n.531+12032G>T
NM_001346557.2:c.531+12032G>T NP_001333486.1:n.531+12032G>T
NR_170598.1:n.1646+12032G>T