Canonical Allele Identifier: CA362742562
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2306068
ClinVar RCV Id: RCV004149196
MyVariant Identifiers: chr6:g.6588974G>T (hg19) chr6:g.6588741G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588741G>T , CM000668.2:g.6588741G>T GRCh38
NC_000006.11:g.6588974G>T , CM000668.1:g.6588974G>T GRCh37
NC_000006.10:g.6533973G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.7G>T (LY86) MANE Select ENSP00000230568.3:p.Gly3Cys
ENST00000230568.4:c.7G>T (LY86) ENSP00000230568.3:p.Gly3Cys
ENST00000379953.6:c.7G>T (LY86) ENSP00000369286.1:p.Gly3Cys
NM_004271.3:c.7G>T (LY86) NP_004262.1:p.Gly3Cys
NR_026970.1:n.196-19252C>A (LY86-AS1)
XM_017011505.1:c.7G>T (LY86) XP_016866994.1:p.Gly3Cys
NM_004271.4:c.7G>T (LY86) MANE Select NP_004262.1:p.Gly3Cys
Search 100 bp 5'
Search 100 bp 3'