Canonical Allele Identifier: CA805660130
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1316865925
MyVariant Identifiers: chr5:g.150240573A>T (hg19) chr5:g.150861011A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150861011A>T , CM000667.2:g.150861011A>T GRCh38
NC_000005.9:g.150240573A>T , CM000667.1:g.150240573A>T GRCh37
NC_000005.8:g.150220766A>T NCBI36
NG_027809.2:g.19489A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+12357A>T
XM_011537641.1:c.531+12357A>T XP_011535943.1:n.531+12357A>T
NM_001346557.1:c.531+12357A>T NP_001333486.1:n.531+12357A>T
NM_001346557.2:c.531+12357A>T NP_001333486.1:n.531+12357A>T
NR_170598.1:n.1646+12357A>T
Search 100 bp 5'
Search 100 bp 3'