Canonical Allele Identifier: CA861404978
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1253612989
gnomAD v3: 9-15120552-G-A
gnomAD v4: 9-15120552-G-A
MyVariant Identifiers: chr9:g.15120550G>A (hg19) chr9:g.15120552G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120552G>A , CM000671.2:g.15120552G>A GRCh38
NC_000009.11:g.15120550G>A , CM000671.1:g.15120550G>A GRCh37
NC_000009.10:g.15110550G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5178C>T
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