Canonical Allele Identifier: CA1121649920
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821544604
gnomAD v3: 9-15120462-C-T
gnomAD v4: 9-15120462-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120462C>T , CM000671.2:g.15120462C>T GRCh38
NC_000009.11:g.15120460C>T , CM000671.1:g.15120460C>T GRCh37
NC_000009.10:g.15110460C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5268G>A
Search 100 bp 5'
Search 100 bp 3'