Canonical Allele Identifier: CA2206128088
Gene: TMEM186 HGNC NCBI
PMM2 HGNC NCBI

Linked Data

dbSNP Id: rs1359678944
gnomAD v4: 16-8797637-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797637A>G , CM000678.2:g.8797637A>G GRCh38
NC_000016.9:g.8891494A>G , CM000678.1:g.8891494A>G GRCh37
NC_000016.8:g.8798995A>G NCBI36
NG_009209.1:g.4825A>G
NG_033146.1:g.5012T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333050.7:c.-23T>C (TMEM186) MANE Select ENSP00000331640.6:n.-23T>C
ENST00000333050.6:c.-23T>C (TMEM186) ENSP00000331640.6:n.-23T>C
ENST00000564869.1:n.6T>C (TMEM186)
ENST00000566983.5:c.-15-4162A>G (PMM2) ENSP00000457956.1:n.-15-4162A>G
NM_015421.3:c.-23T>C (TMEM186) NP_056236.2:n.-23T>C
NM_015421.4:c.-23T>C (TMEM186) MANE Select NP_056236.2:n.-23T>C