Canonical Allele Identifier: CA189418028
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs953227832
gnomAD v3: 9-15120100-T-A
gnomAD v4: 9-15120100-T-A
MyVariant Identifiers: chr9:g.15120100T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120100T>A , CM000671.2:g.15120100T>A GRCh38
NC_000009.11:g.15120098T>A , CM000671.1:g.15120098T>A GRCh37
NC_000009.10:g.15110098T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5630A>T
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