Canonical Allele Identifier: CA447412355
Gene: IRGM HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.150228000G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150848438G>T , CM000667.2:g.150848438G>T GRCh38
NC_000005.9:g.150228000G>T , CM000667.1:g.150228000G>T GRCh37
NC_000005.8:g.150208193G>T NCBI36
NG_027809.1:g.6916G>T
NG_027809.2:g.6916G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000522154.2:c.315G>T MANE Select ENSP00000428220.1:p.Leu105=
ENST00000522154.1:c.315G>T ENSP00000428220.1:p.Leu105=
NM_001145805.1:c.315G>T NP_001139277.1:p.Leu105=
XM_011537641.1:c.315G>T XP_011535943.1:p.Leu105=
NM_001346557.1:c.315G>T NP_001333486.1:p.Leu105=
NM_001346557.2:c.315G>T NP_001333486.1:p.Leu105=
NM_001145805.2:c.315G>T MANE Select NP_001139277.1:p.Leu105=
NR_170598.1:n.1430G>T