Canonical Allele Identifier: CA447412236
Gene: IRGM HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.150227811T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150848249T>C , CM000667.2:g.150848249T>C GRCh38
NC_000005.9:g.150227811T>C , CM000667.1:g.150227811T>C GRCh37
NC_000005.8:g.150208004T>C NCBI36
NG_027809.1:g.6727T>C
NG_027809.2:g.6727T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000522154.2:c.126T>C MANE Select ENSP00000428220.1:p.Ser42=
ENST00000522154.1:c.126T>C ENSP00000428220.1:p.Ser42=
NM_001145805.1:c.126T>C NP_001139277.1:p.Ser42=
XM_011537641.1:c.126T>C XP_011535943.1:p.Ser42=
NM_001346557.1:c.126T>C NP_001333486.1:p.Ser42=
NM_001346557.2:c.126T>C NP_001333486.1:p.Ser42=
NM_001145805.2:c.126T>C MANE Select NP_001139277.1:p.Ser42=
NR_170598.1:n.1241T>C
Search 100 bp 5'
Search 100 bp 3'