Canonical Allele Identifier: CA1835374580
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs555308792
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120448C>A , CM000671.2:g.15120448C>A GRCh38
NC_000009.11:g.15120446C>A , CM000671.1:g.15120446C>A GRCh37
NC_000009.10:g.15110446C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5282G>T
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Search 100 bp 3'