Canonical Allele Identifier: CA1835374341
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821543034

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120231A>G , CM000671.2:g.15120231A>G GRCh38
NC_000009.11:g.15120229A>G , CM000671.1:g.15120229A>G GRCh37
NC_000009.10:g.15110229A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5499T>C