Canonical Allele Identifier: CA563587144
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1235663878

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860611G>A , CM000667.2:g.150860611G>A GRCh38
NC_000005.9:g.150240173G>A , CM000667.1:g.150240173G>A GRCh37
NC_000005.8:g.150220366G>A NCBI36
NG_027809.2:g.19089G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11957G>A
XM_011537641.1:c.531+11957G>A XP_011535943.1:n.531+11957G>A
NM_001346557.1:c.531+11957G>A NP_001333486.1:n.531+11957G>A
NM_001346557.2:c.531+11957G>A NP_001333486.1:n.531+11957G>A
NR_170598.1:n.1646+11957G>A