Canonical Allele Identifier: CA2206128098
Gene: TMEM186 HGNC NCBI
PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797648C= , CM000678.2:g.8797648C= GRCh38
NC_000016.9:g.8891505C= , CM000678.1:g.8891505C= GRCh37
NC_000016.8:g.8799006C= NCBI36
NG_009209.1:g.4836C=
NG_033146.1:g.5001G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333050.6:c.-34G= (TMEM186) ENSP00000331640.6:n.-34G=
ENST00000566983.5:c.-15-4151C= (PMM2) ENSP00000457956.1:n.-15-4151C=
NM_015421.3:c.-34G= (TMEM186) NP_056236.2:n.-34G=