Canonical Allele Identifier: CA697948640
Gene: LHFPL6 HGNC NCBI

Linked Data

dbSNP Id: rs1364543927
MyVariant Identifiers: chr13:g.39903217A>C (hg19) chr13:g.39329080A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39329080A>C , CM000675.2:g.39329080A>C GRCh38
NC_000013.10:g.39903217A>C , CM000675.1:g.39903217A>C GRCh37
NC_000013.9:g.38801217A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000648377.1:c.*82+14774T>G ENSP00000496801.1:n.*82+14774T>G
XR_001749845.1:n.1449+7191T>G
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