Canonical Allele Identifier: CA362742611
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.6589000G>C (hg19) chr6:g.6588767G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588767G>C , CM000668.2:g.6588767G>C GRCh38
NC_000006.11:g.6589000G>C , CM000668.1:g.6589000G>C GRCh37
NC_000006.10:g.6533999G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.33G>C (LY86) MANE Select ENSP00000230568.3:p.Trp11Cys
ENST00000230568.4:c.33G>C (LY86) ENSP00000230568.3:p.Trp11Cys
ENST00000379953.6:c.33G>C (LY86) ENSP00000369286.1:p.Trp11Cys
NM_004271.3:c.33G>C (LY86) NP_004262.1:p.Trp11Cys
NR_026970.1:n.196-19278C>G (LY86-AS1)
XM_017011505.1:c.33G>C (LY86) XP_016866994.1:p.Trp11Cys
NM_004271.4:c.33G>C (LY86) MANE Select NP_004262.1:p.Trp11Cys
Search 100 bp 5'
Search 100 bp 3'