Canonical Allele Identifier: CA1835374694
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1253612989

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120552G>T , CM000671.2:g.15120552G>T GRCh38
NC_000009.11:g.15120550G>T , CM000671.1:g.15120550G>T GRCh37
NC_000009.10:g.15110550G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5178C>A