Canonical Allele Identifier: CA861404945

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs1365956473
• gnomAD v3: 9-15120274-G-A
• gnomAD v4: 9-15120274-G-A
• MyVariant Identifiers: chr9:g.15120272G>A (hg19) ; chr9:g.15120274G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120274G>A , CM000671.2:g.15120274G>A	GRCh38
NC_000009.11:g.15120272G>A , CM000671.1:g.15120272G>A	GRCh37
NC_000009.10:g.15110272G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609203.1:n.549+5456C>T