Canonical Allele Identifier: CA361785280
Gene: IRGM HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.150227914T>C (hg19) chr5:g.150848352T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150848352T>C , CM000667.2:g.150848352T>C GRCh38
NC_000005.9:g.150227914T>C , CM000667.1:g.150227914T>C GRCh37
NC_000005.8:g.150208107T>C NCBI36
NG_027809.1:g.6830T>C
NG_027809.2:g.6830T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000522154.2:c.229T>C MANE Select ENSP00000428220.1:p.Ser77Pro
ENST00000522154.1:c.229T>C ENSP00000428220.1:p.Ser77Pro
NM_001145805.1:c.229T>C NP_001139277.1:p.Ser77Pro
XM_011537641.1:c.229T>C XP_011535943.1:p.Ser77Pro
NM_001346557.1:c.229T>C NP_001333486.1:p.Ser77Pro
NM_001346557.2:c.229T>C NP_001333486.1:p.Ser77Pro
NM_001145805.2:c.229T>C MANE Select NP_001139277.1:p.Ser77Pro
NR_170598.1:n.1344T>C
Search 100 bp 5'
Search 100 bp 3'