Canonical Allele Identifier: CA448646321
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs771803488
MyVariant Identifiers: chr6:g.6589063C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588830C>T , CM000668.2:g.6588830C>T GRCh38
NC_000006.11:g.6589063C>T , CM000668.1:g.6589063C>T GRCh37
NC_000006.10:g.6534062C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.96C>T (LY86) MANE Select ENSP00000230568.3:p.Val32=
ENST00000230568.4:c.96C>T (LY86) ENSP00000230568.3:p.Val32=
ENST00000379953.6:c.96C>T (LY86) ENSP00000369286.1:p.Val32=
NM_004271.3:c.96C>T (LY86) NP_004262.1:p.Val32=
NR_026970.1:n.196-19341G>A (LY86-AS1)
XM_017011505.1:c.96C>T (LY86) XP_016866994.1:p.Val32=
NM_004271.4:c.96C>T (LY86) MANE Select NP_004262.1:p.Val32=