Canonical Allele Identifier: CA586249540
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1354547802
gnomAD v2: 9-15120578-A-G
gnomAD v3: 9-15120580-A-G
gnomAD v4: 9-15120580-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120580A>G , CM000671.2:g.15120580A>G GRCh38
NC_000009.11:g.15120578A>G , CM000671.1:g.15120578A>G GRCh37
NC_000009.10:g.15110578A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5150T>C