Canonical Allele Identifier: CA362742851
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1383011029
gnomAD v2: 6-6589092-A-G
gnomAD v4: 6-6588859-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588859A>G , CM000668.2:g.6588859A>G GRCh38
NC_000006.11:g.6589092A>G , CM000668.1:g.6589092A>G GRCh37
NC_000006.10:g.6534091A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.125A>G (LY86) MANE Select ENSP00000230568.3:p.Tyr42Cys
ENST00000230568.4:c.125A>G (LY86) ENSP00000230568.3:p.Tyr42Cys
ENST00000379953.6:c.125A>G (LY86) ENSP00000369286.1:p.Tyr42Cys
NM_004271.3:c.125A>G (LY86) NP_004262.1:p.Tyr42Cys
NR_026970.1:n.196-19370T>C (LY86-AS1)
XM_017011505.1:c.125A>G (LY86) XP_016866994.1:p.Tyr42Cys
NM_004271.4:c.125A>G (LY86) MANE Select NP_004262.1:p.Tyr42Cys