Canonical Allele Identifier: CA2206128096
Gene: TMEM186 HGNC NCBI
PMM2 HGNC NCBI

Linked Data

dbSNP Id: rs1404073087

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797647A>G , CM000678.2:g.8797647A>G GRCh38
NC_000016.9:g.8891504A>G , CM000678.1:g.8891504A>G GRCh37
NC_000016.8:g.8799005A>G NCBI36
NG_009209.1:g.4835A>G
NG_033146.1:g.5002T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333050.6:c.-33T>C (TMEM186) ENSP00000331640.6:n.-33T>C
ENST00000566983.5:c.-15-4152A>G (PMM2) ENSP00000457956.1:n.-15-4152A>G
NM_015421.3:c.-33T>C (TMEM186) NP_056236.2:n.-33T>C