Canonical Allele Identifier: CA448646347
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1313405027
gnomAD v3: 6-6588854-G-A
gnomAD v4: 6-6588854-G-A
MyVariant Identifiers: chr6:g.6589087G>A (hg19) chr6:g.6588854G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588854G>A , CM000668.2:g.6588854G>A GRCh38
NC_000006.11:g.6589087G>A , CM000668.1:g.6589087G>A GRCh37
NC_000006.10:g.6534086G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.120G>A (LY86) MANE Select ENSP00000230568.3:p.Val40=
ENST00000230568.4:c.120G>A (LY86) ENSP00000230568.3:p.Val40=
ENST00000379953.6:c.120G>A (LY86) ENSP00000369286.1:p.Val40=
NM_004271.3:c.120G>A (LY86) NP_004262.1:p.Val40=
NR_026970.1:n.196-19365C>T (LY86-AS1)
XM_017011505.1:c.120G>A (LY86) XP_016866994.1:p.Val40=
NM_004271.4:c.120G>A (LY86) MANE Select NP_004262.1:p.Val40=
Search 100 bp 5'
Search 100 bp 3'