Canonical Allele Identifier: CA827149980
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1204729192
gnomAD v4: 6-6588479-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588479T>C , CM000668.2:g.6588479T>C GRCh38
NC_000006.11:g.6588712T>C , CM000668.1:g.6588712T>C GRCh37
NC_000006.10:g.6533711T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379953.6:c.-10+29T>C (LY86) ENSP00000369286.1:n.-10+29T>C
NR_026970.1:n.196-18990A>G (LY86-AS1)