Canonical Allele Identifier: CA189418292
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs750630028
MyVariant Identifiers: chr9:g.15120504C>T (hg19) chr9:g.15120506C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120506C>T , CM000671.2:g.15120506C>T GRCh38
NC_000009.11:g.15120504C>T , CM000671.1:g.15120504C>T GRCh37
NC_000009.10:g.15110504C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5224G>A
Search 100 bp 5'
Search 100 bp 3'