Canonical Allele Identifier: CA3624899
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 782469
ClinVar RCV Id: RCV000963862
dbSNP Id: rs74356155
ExAC: 6:6588997 C / T
gnomAD v2: 6-6588997-C-T
gnomAD v3: 6-6588764-C-T
gnomAD v4: 6-6588764-C-T
MyVariant Identifiers: chr6:g.6588997C>T (hg19) chr6:g.6588764C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588764C>T , CM000668.2:g.6588764C>T GRCh38
NC_000006.11:g.6588997C>T , CM000668.1:g.6588997C>T GRCh37
NC_000006.10:g.6533996C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.30C>T (LY86) MANE Select ENSP00000230568.3:p.Leu10=
ENST00000230568.4:c.30C>T (LY86) ENSP00000230568.3:p.Leu10=
ENST00000379953.6:c.30C>T (LY86) ENSP00000369286.1:p.Leu10=
NM_004271.3:c.30C>T (LY86) NP_004262.1:p.Leu10=
NR_026970.1:n.196-19275G>A (LY86-AS1)
XM_017011505.1:c.30C>T (LY86) XP_016866994.1:p.Leu10=
NM_004271.4:c.30C>T (LY86) MANE Select NP_004262.1:p.Leu10=
Search 100 bp 5'
Search 100 bp 3'