Canonical Allele Identifier: CA565308566
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1286652634
gnomAD v2: 6-6588963-C-T
gnomAD v4: 6-6588730-C-T
MyVariant Identifiers: chr6:g.6588963C>T (hg19) chr6:g.6588730C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588730C>T , CM000668.2:g.6588730C>T GRCh38
NC_000006.11:g.6588963C>T , CM000668.1:g.6588963C>T GRCh37
NC_000006.10:g.6533962C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.-5C>T (LY86) MANE Select ENSP00000230568.3:n.-5C>T
ENST00000230568.4:c.-5C>T (LY86) ENSP00000230568.3:n.-5C>T
ENST00000379953.6:c.-5C>T (LY86) ENSP00000369286.1:n.-5C>T
NM_004271.3:c.-5C>T (LY86) NP_004262.1:n.-5C>T
NR_026970.1:n.196-19241G>A (LY86-AS1)
XM_017011505.1:c.-5C>T (LY86) XP_016866994.1:n.-5C>T
NM_004271.4:c.-5C>T (LY86) MANE Select NP_004262.1:n.-5C>T
Search 100 bp 5'
Search 100 bp 3'