Canonical Allele Identifier: CA1835374224
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1588796980

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120116A>C , CM000671.2:g.15120116A>C GRCh38
NC_000009.11:g.15120114A>C , CM000671.1:g.15120114A>C GRCh37
NC_000009.10:g.15110114A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5614T>G