Canonical Allele Identifier: CA1578376374

Linked Data

dbSNP Id: rs1754413302

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122070324T>C , CM000667.2:g.122070324T>C GRCh38
NC_000005.9:g.121406019T>C , CM000667.1:g.121406019T>C GRCh37
NC_000005.8:g.121433918T>C NCBI36
NG_008722.1:g.13037A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000231004.5:c.1132-156A>G (LOX) MANE Select ENSP00000231004.4:n.1132-156A>G
ENST00000639739.2:c.*324-156A>G (LOX) ENSP00000492324.2:n.*324-156A>G
ENST00000231004.4:c.1132-156A>G (LOX) ENSP00000231004.4:n.1132-156A>G
ENST00000503759.5:n.723-156A>G (LOX)
ENST00000504881.1:n.312-4991T>C (SRFBP1)
ENST00000505593.5:n.458-156A>G (LOX)
ENST00000513319.5:n.475-156A>G (LOX)
NM_001178102.1:c.442-156A>G (LOX) NP_001171573.1:n.442-156A>G
NM_001178102.2:c.442-156A>G (LOX) NP_001171573.1:n.442-156A>G
NM_001317073.1:c.241-156A>G (LOX) NP_001304002.1:n.241-156A>G
NM_002317.5:c.1132-156A>G (LOX) NP_002308.2:n.1132-156A>G
NM_002317.6:c.1132-156A>G (LOX) NP_002308.2:n.1132-156A>G
XM_017009111.2:c.1106-4991T>C (SRFBP1) XP_016864600.2:n.1106-4991T>C
NM_002317.7:c.1132-156A>G (LOX) MANE Select NP_002308.2:n.1132-156A>G