Canonical Allele Identifier: CA565308542
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1423689126
gnomAD v2: 6-6588919-C-CT
gnomAD v4: 6-6588686-C-CT

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588691dup , CM000668.2:g.6588691dup GRCh38
NC_000006.11:g.6588924dup , CM000668.1:g.6588924dup GRCh37
NC_000006.10:g.6533923dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.4:c.-44dup (LY86) ENSP00000230568.3:n.-44dup
ENST00000379953.6:c.-9-35dup (LY86) ENSP00000369286.1:n.-9-35dup
NR_026970.1:n.196-19198dup (LY86-AS1)
XM_017011505.1:c.-44dup (LY86) XP_016866994.1:n.-44dup