Canonical Allele Identifier: CA3624901
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs771510951
gnomAD v2: 6-6589017-G-C
gnomAD v4: 6-6588784-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588784G>C , CM000668.2:g.6588784G>C GRCh38
NC_000006.11:g.6589017G>C , CM000668.1:g.6589017G>C GRCh37
NC_000006.10:g.6534016G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.50G>C (LY86) MANE Select ENSP00000230568.3:p.Ser17Thr
ENST00000230568.4:c.50G>C (LY86) ENSP00000230568.3:p.Ser17Thr
ENST00000379953.6:c.50G>C (LY86) ENSP00000369286.1:p.Ser17Thr
NM_004271.3:c.50G>C (LY86) NP_004262.1:p.Ser17Thr
NR_026970.1:n.196-19295C>G (LY86-AS1)
XM_017011505.1:c.50G>C (LY86) XP_016866994.1:p.Ser17Thr
NM_004271.4:c.50G>C (LY86) MANE Select NP_004262.1:p.Ser17Thr