Canonical Allele Identifier: CA447412228
Gene: IRGM HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.150227802A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150848240A>C , CM000667.2:g.150848240A>C GRCh38
NC_000005.9:g.150227802A>C , CM000667.1:g.150227802A>C GRCh37
NC_000005.8:g.150207995A>C NCBI36
NG_027809.1:g.6718A>C
NG_027809.2:g.6718A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000522154.2:c.117A>C MANE Select ENSP00000428220.1:p.Ala39=
ENST00000522154.1:c.117A>C ENSP00000428220.1:p.Ala39=
NM_001145805.1:c.117A>C NP_001139277.1:p.Ala39=
XM_011537641.1:c.117A>C XP_011535943.1:p.Ala39=
NM_001346557.1:c.117A>C NP_001333486.1:p.Ala39=
NM_001346557.2:c.117A>C NP_001333486.1:p.Ala39=
NM_001145805.2:c.117A>C MANE Select NP_001139277.1:p.Ala39=
NR_170598.1:n.1232A>C