Canonical Allele Identifier: CA405815921
Gene: CLC HGNC NCBI

Linked Data

gnomAD v4: 19-39735018-C-A
MyVariant Identifiers: chr19:g.40225658C>A (hg19) chr19:g.39735018C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39735018C>A , CM000681.2:g.39735018C>A GRCh38
NC_000019.9:g.40225658C>A , CM000681.1:g.40225658C>A GRCh37
NC_000019.8:g.44917498C>A NCBI36
NG_046978.1:g.8012G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000221804.5:c.71G>T MANE Select ENSP00000221804.3:p.Gly24Val
ENST00000221804.4:c.71G>T ENSP00000221804.3:p.Gly24Val
NM_001828.5:c.71G>T NP_001819.2:p.Gly24Val
NM_001828.6:c.71G>T MANE Select NP_001819.2:p.Gly24Val
Search 100 bp 5'
Search 100 bp 3'