ClinGen Allele Registry
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Canonical Allele Identifier:
CA11377235
Gene: TMED10P2
HGNC
NCBI
Linked Data
dbSNP Id:
rs9854612
gnomAD v2:
3-128257214-G-A
gnomAD v3:
3-128538371-G-A
gnomAD v4:
3-128538371-G-A
MyVariant Identifiers:
chr3:g.128257214G>A (hg19)
chr3:g.128538371G>A (hg38)
JSON-LD
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'