Canonical Allele Identifier: CA1085638372
Gene: LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1334710
gnomAD v3: 6-6583488-G-T
gnomAD v4: 6-6583488-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6583488G>T , CM000668.2:g.6583488G>T GRCh38
NC_000006.11:g.6583721G>T , CM000668.1:g.6583721G>T GRCh37
NC_000006.10:g.6528720G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_026970.1:n.196-13999C>A