Canonical Allele Identifier: CA3624877
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs572121114
ExAC: 6:6588948 G / T
gnomAD v2: 6-6588948-G-T
gnomAD v3: 6-6588715-G-T
gnomAD v4: 6-6588715-G-T
MyVariant Identifiers: chr6:g.6588948G>T (hg19) chr6:g.6588715G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588715G>T , CM000668.2:g.6588715G>T GRCh38
NC_000006.11:g.6588948G>T , CM000668.1:g.6588948G>T GRCh37
NC_000006.10:g.6533947G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.4:c.-20G>T (LY86) ENSP00000230568.3:n.-20G>T
ENST00000379953.6:c.-9-11G>T (LY86) ENSP00000369286.1:n.-9-11G>T
NM_004271.3:c.-20G>T (LY86) NP_004262.1:n.-20G>T
NR_026970.1:n.196-19226C>A (LY86-AS1)
XM_017011505.1:c.-20G>T (LY86) XP_016866994.1:n.-20G>T
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