Canonical Allele Identifier: CA10626698
Gene: LHFPL5 HGNC NCBI

Linked Data

ClinVar Variation Id: 356485
ClinVar RCV Id: RCV000279683
dbSNP Id: rs540528658
gnomAD v2: 6-35773355-C-T
gnomAD v3: 6-35805578-C-T
gnomAD v4: 6-35805578-C-T
MyVariant Identifiers: chr6:g.35773355C>T (hg19) chr6:g.35805578C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35805578C>T , CM000668.2:g.35805578C>T GRCh38
NC_000006.11:g.35773355C>T , CM000668.1:g.35773355C>T GRCh37
NC_000006.10:g.35881333C>T NCBI36
NG_012184.1:g.5285C>T
NG_012184.2:g.5285C>T
NG_012184.3:g.13373C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360215.3:c.-93C>T MANE Select ENSP00000353346.1:n.-93C>T
ENST00000651132.1:c.-93C>T ENSP00000498322.1:n.-93C>T
ENST00000651676.1:c.-93C>T ENSP00000498699.1:n.-93C>T
ENST00000651994.1:c.-93C>T ENSP00000498310.1:n.-93C>T
ENST00000360215.2:c.-93C>T ENSP00000353346.1:n.-93C>T
NM_182548.3:c.-93C>T NP_872354.1:n.-93C>T
XM_011514403.1:c.-93C>T XP_011512705.1:n.-93C>T
NM_182548.4:c.-93C>T MANE Select NP_872354.1:n.-93C>T
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