Canonical Allele Identifier: CA1608139199
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588489A= , CM000668.2:g.6588489A= GRCh38
NC_000006.11:g.6588722A= , CM000668.1:g.6588722A= GRCh37
NC_000006.10:g.6533721A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379953.6:c.-10+39A= (LY86) ENSP00000369286.1:n.-10+39A=
NR_026970.1:n.196-19000T= (LY86-AS1)