Canonical Allele Identifier: CA3624904
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs532377967
ExAC: 6:6589026 G / T
gnomAD v2: 6-6589026-G-T
gnomAD v3: 6-6588793-G-T
gnomAD v4: 6-6588793-G-T
MyVariant Identifiers: chr6:g.6589026G>T (hg19) chr6:g.6588793G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588793G>T , CM000668.2:g.6588793G>T GRCh38
NC_000006.11:g.6589026G>T , CM000668.1:g.6589026G>T GRCh37
NC_000006.10:g.6534025G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.59G>T (LY86) MANE Select ENSP00000230568.3:p.Gly20Val
ENST00000230568.4:c.59G>T (LY86) ENSP00000230568.3:p.Gly20Val
ENST00000379953.6:c.59G>T (LY86) ENSP00000369286.1:p.Gly20Val
NM_004271.3:c.59G>T (LY86) NP_004262.1:p.Gly20Val
NR_026970.1:n.196-19304C>A (LY86-AS1)
XM_017011505.1:c.59G>T (LY86) XP_016866994.1:p.Gly20Val
NM_004271.4:c.59G>T (LY86) MANE Select NP_004262.1:p.Gly20Val
Search 100 bp 5'
Search 100 bp 3'