Canonical Allele Identifier: CA3624926
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2531192
ClinVar RCV Id: RCV004299573
dbSNP Id: rs530215928
ExAC: 6:6589076 G / A
gnomAD v2: 6-6589076-G-A
gnomAD v3: 6-6588843-G-A
gnomAD v4: 6-6588843-G-A
MyVariant Identifiers: chr6:g.6589076G>A (hg19) chr6:g.6588843G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588843G>A , CM000668.2:g.6588843G>A GRCh38
NC_000006.11:g.6589076G>A , CM000668.1:g.6589076G>A GRCh37
NC_000006.10:g.6534075G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.109G>A (LY86) MANE Select ENSP00000230568.3:p.Gly37Ser
ENST00000230568.4:c.109G>A (LY86) ENSP00000230568.3:p.Gly37Ser
ENST00000379953.6:c.109G>A (LY86) ENSP00000369286.1:p.Gly37Ser
NM_004271.3:c.109G>A (LY86) NP_004262.1:p.Gly37Ser
NR_026970.1:n.196-19354C>T (LY86-AS1)
XM_017011505.1:c.109G>A (LY86) XP_016866994.1:p.Gly37Ser
NM_004271.4:c.109G>A (LY86) MANE Select NP_004262.1:p.Gly37Ser
Search 100 bp 5'
Search 100 bp 3'