Canonical Allele Identifier: CA134433543
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs977012219
gnomAD v3: 6-6588677-T-G
gnomAD v4: 6-6588677-T-G
MyVariant Identifiers: chr6:g.6588910T>G (hg19) chr6:g.6588677T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588677T>G , CM000668.2:g.6588677T>G GRCh38
NC_000006.11:g.6588910T>G , CM000668.1:g.6588910T>G GRCh37
NC_000006.10:g.6533909T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.4:c.-58T>G (LY86) ENSP00000230568.3:n.-58T>G
ENST00000379953.6:c.-9-49T>G (LY86) ENSP00000369286.1:n.-9-49T>G
NR_026970.1:n.196-19188A>C (LY86-AS1)
XM_017011505.1:c.-58T>G (LY86) XP_016866994.1:n.-58T>G
Search 100 bp 5'
Search 100 bp 3'