Canonical Allele Identifier: CA405815944
Gene: CLC HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.40225659C>T (hg19) chr19:g.39735019C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39735019C>T , CM000681.2:g.39735019C>T GRCh38
NC_000019.9:g.40225659C>T , CM000681.1:g.40225659C>T GRCh37
NC_000019.8:g.44917499C>T NCBI36
NG_046978.1:g.8011G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000221804.5:c.70G>A MANE Select ENSP00000221804.3:p.Gly24Arg
ENST00000221804.4:c.70G>A ENSP00000221804.3:p.Gly24Arg
NM_001828.5:c.70G>A NP_001819.2:p.Gly24Arg
NM_001828.6:c.70G>A MANE Select NP_001819.2:p.Gly24Arg
Search 100 bp 5'
Search 100 bp 3'