Canonical Allele Identifier: CA1835374323
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821542862

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120199C>T , CM000671.2:g.15120199C>T GRCh38
NC_000009.11:g.15120197C>T , CM000671.1:g.15120197C>T GRCh37
NC_000009.10:g.15110197C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5531G>A