Canonical Allele Identifier: CA2710196708
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs2113263809

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860641G>A , CM000667.2:g.150860641G>A GRCh38
NC_000005.9:g.150240203G>A , CM000667.1:g.150240203G>A GRCh37
NC_000005.8:g.150220396G>A NCBI36
NG_027809.2:g.19119G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11987G>A
XM_011537641.1:c.531+11987G>A XP_011535943.1:n.531+11987G>A
NM_001346557.1:c.531+11987G>A NP_001333486.1:n.531+11987G>A
NM_001346557.2:c.531+11987G>A NP_001333486.1:n.531+11987G>A
NR_170598.1:n.1646+11987G>A