Canonical Allele Identifier: CA2718931816
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs2118116043

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120195T>C , CM000671.2:g.15120195T>C GRCh38
NC_000009.11:g.15120193T>C , CM000671.1:g.15120193T>C GRCh37
NC_000009.10:g.15110193T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5535A>G