Canonical Allele Identifier: CA609313658
Gene: LHFPL6 HGNC NCBI

Linked Data

dbSNP Id: rs1388465999
gnomAD v2: 13-39903102-T-C
gnomAD v3: 13-39328965-T-C
gnomAD v4: 13-39328965-T-C
MyVariant Identifiers: chr13:g.39903102T>C (hg19) chr13:g.39328965T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39328965T>C , CM000675.2:g.39328965T>C GRCh38
NC_000013.10:g.39903102T>C , CM000675.1:g.39903102T>C GRCh37
NC_000013.9:g.38801102T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648377.1:c.*82+14889A>G ENSP00000496801.1:n.*82+14889A>G
XR_001749845.1:n.1449+7306A>G
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