Canonical Allele Identifier: CA1085646910
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1760420021
gnomAD v3: 6-6588456-T-G
gnomAD v4: 6-6588456-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588456T>G , CM000668.2:g.6588456T>G GRCh38
NC_000006.11:g.6588689T>G , CM000668.1:g.6588689T>G GRCh37
NC_000006.10:g.6533688T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379953.6:c.-10+6T>G (LY86) ENSP00000369286.1:n.-10+6T>G
NR_026970.1:n.196-18967A>C (LY86-AS1)