Canonical Allele Identifier: CA448646358
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1760436008
gnomAD v3: 6-6588860-C-T
gnomAD v4: 6-6588860-C-T
MyVariant Identifiers: chr6:g.6589093C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588860C>T , CM000668.2:g.6588860C>T GRCh38
NC_000006.11:g.6589093C>T , CM000668.1:g.6589093C>T GRCh37
NC_000006.10:g.6534092C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.126C>T (LY86) MANE Select ENSP00000230568.3:p.Tyr42=
ENST00000230568.4:c.126C>T (LY86) ENSP00000230568.3:p.Tyr42=
ENST00000379953.6:c.126C>T (LY86) ENSP00000369286.1:p.Tyr42=
NM_004271.3:c.126C>T (LY86) NP_004262.1:p.Tyr42=
NR_026970.1:n.196-19371G>A (LY86-AS1)
XM_017011505.1:c.126C>T (LY86) XP_016866994.1:p.Tyr42=
NM_004271.4:c.126C>T (LY86) MANE Select NP_004262.1:p.Tyr42=
Search 100 bp 5'
Search 100 bp 3'