Canonical Allele Identifier: CA189418381
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs372188434
MyVariant Identifiers: chr9:g.15120601C>A (hg19) chr9:g.15120603C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120603C>A , CM000671.2:g.15120603C>A GRCh38
NC_000009.11:g.15120601C>A , CM000671.1:g.15120601C>A GRCh37
NC_000009.10:g.15110601C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5127G>T
Search 100 bp 5'
Search 100 bp 3'