Canonical Allele Identifier: CA11377235
Gene: TMED10P2 HGNC NCBI
COSMIC:
COSN19629458 (not active)
MyVariant.info:
GRCh38 chr3:g.128538371G>A
GRCh37 chr3:g.128257214G>A
gnomAD v2:
3:128257214 G / A
gnomAD v3:
3:128538371 G / A
gnomAD v4:
chr3-128538371-G-A
Joint Max Group AF 0.59658587 (AFR)
Genomes Max Group AF 0.59500703 (AFR)
Exomes Max Group AF 0.59334757 (AFR)
dbSNP:
9854612
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128538371G>A , CM000665.2:g.128538371G>A GRCh38
NC_000003.11:g.128257214G>A , CM000665.1:g.128257214G>A GRCh37
NC_000003.10:g.129739904G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474255.1:n.352G>A
Search 100 bp 5'
Search 100 bp 3'