Canonical Allele Identifier: CA360876913
Gene: LOX HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.121413361G>C (hg19) chr5:g.122077666G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122077666G>C , CM000667.2:g.122077666G>C GRCh38
NC_000005.9:g.121413361G>C , CM000667.1:g.121413361G>C GRCh37
NC_000005.8:g.121441260G>C NCBI36
NG_008722.1:g.5695C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000231004.5:c.320C>G MANE Select ENSP00000231004.4:p.Ala107Gly
ENST00000639739.2:c.320C>G ENSP00000492324.2:p.Ala107Gly
ENST00000231004.4:c.320C>G ENSP00000231004.4:p.Ala107Gly
NM_002317.5:c.320C>G NP_002308.2:p.Ala107Gly
NM_002317.6:c.320C>G NP_002308.2:p.Ala107Gly
NM_002317.7:c.320C>G MANE Select NP_002308.2:p.Ala107Gly
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