Canonical Allele Identifier: CA2592380127
Gene: CLCN3P1 HGNC NCBI

Linked Data

gnomAD v3: 9-15120324-C-T
gnomAD v4: 9-15120324-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120324C>T , CM000671.2:g.15120324C>T GRCh38
NC_000009.11:g.15120322C>T , CM000671.1:g.15120322C>T GRCh37
NC_000009.10:g.15110322C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5406G>A