Canonical Allele Identifier: CA1121649937
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821545344

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120551_15120554del , CM000671.2:g.15120551_15120554del GRCh38
NC_000009.11:g.15120549_15120552del , CM000671.1:g.15120549_15120552del GRCh37
NC_000009.10:g.15110549_15110552del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5176_549+5179del