Canonical Allele Identifier: CA1748898458
Gene: CLCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1563091627

Genomic Alleles

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

Transcript Alleles

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