Canonical Allele Identifier: CA620726898
Gene: TMEM186 HGNC NCBI
PMM2 HGNC NCBI

Linked Data

dbSNP Id: rs1404073087
gnomAD v2: 16-8891504-A-T
gnomAD v3: 16-8797647-A-T
gnomAD v4: 16-8797647-A-T

Genomic Alleles

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

Transcript Alleles

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