Canonical Allele Identifier: CA1835374333
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs991427028

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120221C>G , CM000671.2:g.15120221C>G GRCh38
NC_000009.11:g.15120219C>G , CM000671.1:g.15120219C>G GRCh37
NC_000009.10:g.15110219C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5509G>C