Canonical Allele Identifier: CA1748898459
Gene: CLCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1563091627
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143352036G>A , CM000669.2:g.143352036G>A GRCh38
NC_000007.13:g.143049129G>A , CM000669.1:g.143049129G>A GRCh37
NC_000007.12:g.142759251G>A NCBI36
NG_009815.1:g.40911G>A
NG_009815.2:g.40911G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650516.2:c.*71G>A ENSP00000498052.2:n.*71G>A
ENST00000343257.7:c.*71G>A MANE Select ENSP00000339867.2:n.*71G>A
ENST00000343257.6:c.*71G>A ENSP00000339867.2:n.*71G>A
XM_011515781.1:c.*71G>A XP_011514083.1:n.*71G>A
XM_011515782.1:c.*71G>A XP_011514084.1:n.*71G>A
NM_000083.3:c.*71G>A MANE Select NP_000074.3:n.*71G>A
NR_046453.2:n.2993G>A
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