Canonical Allele Identifier: CA565308525
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1244123138
gnomAD v2: 6-6588727-A-C
gnomAD v3: 6-6588494-A-C
gnomAD v4: 6-6588494-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588494A>C , CM000668.2:g.6588494A>C GRCh38
NC_000006.11:g.6588727A>C , CM000668.1:g.6588727A>C GRCh37
NC_000006.10:g.6533726A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379953.6:c.-10+44A>C (LY86) ENSP00000369286.1:n.-10+44A>C
NR_026970.1:n.196-19005T>G (LY86-AS1)