Canonical Allele Identifier: CA362742587
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1760430402
gnomAD v4: 6-6588756-C-G
MyVariant Identifiers: chr6:g.6588989C>G (hg19) chr6:g.6588756C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588756C>G , CM000668.2:g.6588756C>G GRCh38
NC_000006.11:g.6588989C>G , CM000668.1:g.6588989C>G GRCh37
NC_000006.10:g.6533988C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.22C>G (LY86) MANE Select ENSP00000230568.3:p.Leu8Val
ENST00000230568.4:c.22C>G (LY86) ENSP00000230568.3:p.Leu8Val
ENST00000379953.6:c.22C>G (LY86) ENSP00000369286.1:p.Leu8Val
NM_004271.3:c.22C>G (LY86) NP_004262.1:p.Leu8Val
NR_026970.1:n.196-19267G>C (LY86-AS1)
XM_017011505.1:c.22C>G (LY86) XP_016866994.1:p.Leu8Val
NM_004271.4:c.22C>G (LY86) MANE Select NP_004262.1:p.Leu8Val
Search 100 bp 5'
Search 100 bp 3'