Canonical Allele Identifier: CA2718925706
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs2118117200
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120642T>A , CM000671.2:g.15120642T>A GRCh38
NC_000009.11:g.15120640T>A , CM000671.1:g.15120640T>A GRCh37
NC_000009.10:g.15110640T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5088A>T
Search 100 bp 5'
Search 100 bp 3'