Canonical Allele Identifier: CA620726900

Gene: TMEM186 PMM2

Linked Data

• dbSNP Id: rs1279036064
• gnomAD v2: 16-8891505-C-A
• gnomAD v3: 16-8797648-C-A
• gnomAD v4: 16-8797648-C-A
• MyVariant Identifiers: chr16:g.8891505C>A (hg19) ; chr16:g.8797648C>A (hg38)

Genomic Alleles

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

Transcript Alleles

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