Canonical Allele Identifier: CA3384063
Gene: LOX HGNC NCBI

Linked Data

dbSNP Id: rs769717725
ExAC: 5:121413357 G / A
gnomAD v2: 5-121413357-G-A
gnomAD v4: 5-122077662-G-A
MyVariant Identifiers: chr5:g.121413357G>A (hg19) chr5:g.122077662G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122077662G>A , CM000667.2:g.122077662G>A GRCh38
NC_000005.9:g.121413357G>A , CM000667.1:g.121413357G>A GRCh37
NC_000005.8:g.121441256G>A NCBI36
NG_008722.1:g.5699C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000231004.5:c.324C>T MANE Select ENSP00000231004.4:p.Gly108=
ENST00000639739.2:c.324C>T ENSP00000492324.2:p.Gly108=
ENST00000231004.4:c.324C>T ENSP00000231004.4:p.Gly108=
NM_002317.5:c.324C>T NP_002308.2:p.Gly108=
NM_002317.6:c.324C>T NP_002308.2:p.Gly108=
NM_002317.7:c.324C>T MANE Select NP_002308.2:p.Gly108=
Search 100 bp 5'
Search 100 bp 3'