Canonical Allele Identifier: CA1835374617
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821544800

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120492A>G , CM000671.2:g.15120492A>G GRCh38
NC_000009.11:g.15120490A>G , CM000671.1:g.15120490A>G GRCh37
NC_000009.10:g.15110490A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5238T>C