Canonical Allele Identifier: CA405815882
Gene: CLC HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.40225652G>A (hg19) chr19:g.39735012G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39735012G>A , CM000681.2:g.39735012G>A GRCh38
NC_000019.9:g.40225652G>A , CM000681.1:g.40225652G>A GRCh37
NC_000019.8:g.44917492G>A NCBI36
NG_046978.1:g.8018C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000221804.5:c.77C>T MANE Select ENSP00000221804.3:p.Pro26Leu
ENST00000221804.4:c.77C>T ENSP00000221804.3:p.Pro26Leu
NM_001828.5:c.77C>T NP_001819.2:p.Pro26Leu
NM_001828.6:c.77C>T MANE Select NP_001819.2:p.Pro26Leu
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