Canonical Allele Identifier: CA861404958

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs1220162500
• MyVariant Identifiers: chr9:g.15120386C>T (hg19) ; chr9:g.15120388C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120388C>T , CM000671.2:g.15120388C>T	GRCh38
NC_000009.11:g.15120386C>T , CM000671.1:g.15120386C>T	GRCh37
NC_000009.10:g.15110386C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609203.1:n.549+5342G>A