Canonical Allele Identifier: CA3624914
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs749164873
ExAC: 6:6589052 A / G
gnomAD v3: 6-6588819-A-G
gnomAD v4: 6-6588819-A-G
MyVariant Identifiers: chr6:g.6589052A>G (hg19) chr6:g.6588819A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588819A>G , CM000668.2:g.6588819A>G GRCh38
NC_000006.11:g.6589052A>G , CM000668.1:g.6589052A>G GRCh37
NC_000006.10:g.6534051A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.85A>G (LY86) MANE Select ENSP00000230568.3:p.Thr29Ala
ENST00000230568.4:c.85A>G (LY86) ENSP00000230568.3:p.Thr29Ala
ENST00000379953.6:c.85A>G (LY86) ENSP00000369286.1:p.Thr29Ala
NM_004271.3:c.85A>G (LY86) NP_004262.1:p.Thr29Ala
NR_026970.1:n.196-19330T>C (LY86-AS1)
XM_017011505.1:c.85A>G (LY86) XP_016866994.1:p.Thr29Ala
NM_004271.4:c.85A>G (LY86) MANE Select NP_004262.1:p.Thr29Ala
Search 100 bp 5'
Search 100 bp 3'