Canonical Allele Identifier: CA10623730
Gene: LHFPL5 HGNC NCBI

Linked Data

ClinVar Variation Id: 356486
ClinVar RCV Id: RCV000334847
dbSNP Id: rs41270084
gnomAD v2: 6-35773385-C-G
gnomAD v3: 6-35805608-C-G
gnomAD v4: 6-35805608-C-G
MyVariant Identifiers: chr6:g.35773385C>G (hg19) chr6:g.35805608C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35805608C>G , CM000668.2:g.35805608C>G GRCh38
NC_000006.11:g.35773385C>G , CM000668.1:g.35773385C>G GRCh37
NC_000006.10:g.35881363C>G NCBI36
NG_012184.1:g.5315C>G
NG_012184.2:g.5315C>G
NG_012184.3:g.13403C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.-63C>G MANE Select ENSP00000353346.1:n.-63C>G
ENST00000651132.1:c.-63C>G ENSP00000498322.1:n.-63C>G
ENST00000651676.1:c.-63C>G ENSP00000498699.1:n.-63C>G
ENST00000651994.1:c.-63C>G ENSP00000498310.1:n.-63C>G
ENST00000360215.2:c.-63C>G ENSP00000353346.1:n.-63C>G
NM_182548.3:c.-63C>G NP_872354.1:n.-63C>G
XM_011514403.1:c.-63C>G XP_011512705.1:n.-63C>G
NM_182548.4:c.-63C>G MANE Select NP_872354.1:n.-63C>G
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