Canonical Allele Identifier: CA134433527
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs567521006
gnomAD v3: 6-6588576-C-T
gnomAD v4: 6-6588576-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588576C>T , CM000668.2:g.6588576C>T GRCh38
NC_000006.11:g.6588809C>T , CM000668.1:g.6588809C>T GRCh37
NC_000006.10:g.6533808C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379953.6:c.-10+126C>T (LY86) ENSP00000369286.1:n.-10+126C>T
NR_026970.1:n.196-19087G>A (LY86-AS1)