Canonical Allele Identifier: CA1835374752
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1564287238
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120622T>A , CM000671.2:g.15120622T>A GRCh38
NC_000009.11:g.15120620T>A , CM000671.1:g.15120620T>A GRCh37
NC_000009.10:g.15110620T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5108A>T
Search 100 bp 5'
Search 100 bp 3'