Canonical Allele Identifier: CA446220218
Gene: LOX HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.121413369C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122077674C>A , CM000667.2:g.122077674C>A GRCh38
NC_000005.9:g.121413369C>A , CM000667.1:g.121413369C>A GRCh37
NC_000005.8:g.121441268C>A NCBI36
NG_008722.1:g.5687G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231004.5:c.312G>T MANE Select ENSP00000231004.4:p.Thr104=
ENST00000639739.2:c.312G>T ENSP00000492324.2:p.Thr104=
ENST00000231004.4:c.312G>T ENSP00000231004.4:p.Thr104=
NM_002317.5:c.312G>T NP_002308.2:p.Thr104=
NM_002317.6:c.312G>T NP_002308.2:p.Thr104=
NM_002317.7:c.312G>T MANE Select NP_002308.2:p.Thr104=