Canonical Allele Identifier: CA697948533
Gene: LHFPL6 HGNC NCBI

Linked Data

dbSNP Id: rs1443681685
gnomAD v3: 13-39328879-T-C
gnomAD v4: 13-39328879-T-C
MyVariant Identifiers: chr13:g.39903016T>C (hg19) chr13:g.39328879T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39328879T>C , CM000675.2:g.39328879T>C GRCh38
NC_000013.10:g.39903016T>C , CM000675.1:g.39903016T>C GRCh37
NC_000013.9:g.38801016T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648377.1:c.*82+14975A>G ENSP00000496801.1:n.*82+14975A>G
XR_001749845.1:n.1449+7392A>G
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