Canonical Allele Identifier: CA134433554
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs374594594
gnomAD v4: 6-6588862-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588862A>G , CM000668.2:g.6588862A>G GRCh38
NC_000006.11:g.6589095A>G , CM000668.1:g.6589095A>G GRCh37
NC_000006.10:g.6534094A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.128A>G (LY86) MANE Select ENSP00000230568.3:p.Gln43Arg
ENST00000230568.4:c.128A>G (LY86) ENSP00000230568.3:p.Gln43Arg
ENST00000379953.6:c.128A>G (LY86) ENSP00000369286.1:p.Gln43Arg
NM_004271.3:c.128A>G (LY86) NP_004262.1:p.Gln43Arg
NR_026970.1:n.196-19373T>C (LY86-AS1)
XM_017011505.1:c.128A>G (LY86) XP_016866994.1:p.Gln43Arg
NM_004271.4:c.128A>G (LY86) MANE Select NP_004262.1:p.Gln43Arg