Canonical Allele Identifier: CA360877515
Gene: LOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1449797
ClinVar RCV Id: RCV002014606
dbSNP Id: rs1414622659
gnomAD v2: 5-121413464-C-T
gnomAD v4: 5-122077769-C-T
MyVariant Identifiers: chr5:g.121413464C>T (hg19) chr5:g.122077769C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122077769C>T , CM000667.2:g.122077769C>T GRCh38
NC_000005.9:g.121413464C>T , CM000667.1:g.121413464C>T GRCh37
NC_000005.8:g.121441363C>T NCBI36
NG_008722.1:g.5592G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.217G>A MANE Select ENSP00000231004.4:p.Gly73Ser
ENST00000639739.2:c.217G>A ENSP00000492324.2:p.Gly73Ser
ENST00000231004.4:c.217G>A ENSP00000231004.4:p.Gly73Ser
NM_002317.5:c.217G>A NP_002308.2:p.Gly73Ser
NM_002317.6:c.217G>A NP_002308.2:p.Gly73Ser
NM_002317.7:c.217G>A MANE Select NP_002308.2:p.Gly73Ser
Search 100 bp 5'
Search 100 bp 3'