Canonical Allele Identifier: CA2511195967
Gene: CLCN3P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120108T>G , CM000671.2:g.15120108T>G GRCh38
NC_000009.11:g.15120106T>G , CM000671.1:g.15120106T>G GRCh37
NC_000009.10:g.15110106T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5622A>C