Canonical Allele Identifier: CA507446977
Gene: CLC HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.40225656G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39735016G>T , CM000681.2:g.39735016G>T GRCh38
NC_000019.9:g.40225656G>T , CM000681.1:g.40225656G>T GRCh37
NC_000019.8:g.44917496G>T NCBI36
NG_046978.1:g.8014C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000221804.5:c.73C>A MANE Select ENSP00000221804.3:p.Arg25=
ENST00000221804.4:c.73C>A ENSP00000221804.3:p.Arg25=
NM_001828.5:c.73C>A NP_001819.2:p.Arg25=
NM_001828.6:c.73C>A MANE Select NP_001819.2:p.Arg25=
Search 100 bp 5'
Search 100 bp 3'