Canonical Allele Identifier: CA1121649832
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821541731
gnomAD v3: 9-15120093-A-T
gnomAD v4: 9-15120093-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120093A>T , CM000671.2:g.15120093A>T GRCh38
NC_000009.11:g.15120091A>T , CM000671.1:g.15120091A>T GRCh37
NC_000009.10:g.15110091A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5637T>A