Canonical Allele Identifier: CA168212765

Gene: CLCN1

Linked Data

• dbSNP Id: rs1013781919
• gnomAD v4: 7-143331029-C-G
• MyVariant Identifiers: chr7:g.143028122C>G (hg19) ; chr7:g.143331029C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143331029C>G , CM000669.2:g.143331029C>G	GRCh38
NC_000007.13:g.143028122C>G , CM000669.1:g.143028122C>G	GRCh37
NC_000007.12:g.142738244C>G	NCBI36
NG_009815.1:g.19904C>G
NG_009815.2:g.19904C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.979+132C>G	ENSP00000498052.2:n.979+132C>G
ENST00000343257.7:c.979+132C>G MANE Select	ENSP00000339867.2:n.979+132C>G
ENST00000432192.6:c.803+132C>G
ENST00000343257.6:c.979+132C>G	ENSP00000339867.2:n.979+132C>G
NM_000083.2:c.979+132C>G	NP_000074.2:n.979+132C>G
NR_046453.1:n.1069+132C>G
XM_011515781.1:c.979+132C>G	XP_011514083.1:n.979+132C>G
XM_017011739.1:c.529+132C>G	XP_016867228.1:n.529+132C>G
XM_017011740.1:c.529+132C>G	XP_016867229.1:n.529+132C>G
NM_000083.3:c.979+132C>G MANE Select	NP_000074.3:n.979+132C>G
NR_046453.2:n.1084+132C>G