Canonical Allele Identifier: CA134437222
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs7740529

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6610376C>T , CM000668.2:g.6610376C>T GRCh38
NC_000006.11:g.6610609C>T , CM000668.1:g.6610609C>T GRCh37
NC_000006.10:g.6555608C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000230568.5:c.137-14550C>T (LY86) MANE Select ENSP00000230568.3:p.=
ENST00000230568.4:c.137-14550C>T ENSP00000230568.3:p.=
ENST00000379953.6:c.137-14550C>T ENSP00000369286.1:p.=
NM_004271.3:c.137-14550C>T (LY86) NP_004262.1:p.=
NR_026970.1:n.195+12256G>A (LY86-AS1)
XM_017011505.1:c.137-14550C>T (LY86) XP_016866994.1:p.=
NM_004271.4:c.137-14550C>T (LY86) MANE Select NP_004262.1:p.=