Canonical Allele Identifier: CA3624931
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs201912095
ExAC: 6:6589102 C / T
gnomAD v2: 6-6589102-C-T
gnomAD v3: 6-6588869-C-T
gnomAD v4: 6-6588869-C-T
MyVariant Identifiers: chr6:g.6589102C>T (hg19) chr6:g.6588869C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588869C>T , CM000668.2:g.6588869C>T GRCh38
NC_000006.11:g.6589102C>T , CM000668.1:g.6589102C>T GRCh37
NC_000006.10:g.6534101C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.135C>T (LY86) MANE Select ENSP00000230568.3:p.Cys45=
ENST00000230568.4:c.135C>T (LY86) ENSP00000230568.3:p.Cys45=
ENST00000379953.6:c.135C>T (LY86) ENSP00000369286.1:p.Cys45=
NM_004271.3:c.135C>T (LY86) NP_004262.1:p.Cys45=
NR_026970.1:n.196-19380G>A (LY86-AS1)
XM_017011505.1:c.135C>T (LY86) XP_016866994.1:p.Cys45=
NM_004271.4:c.135C>T (LY86) MANE Select NP_004262.1:p.Cys45=
Search 100 bp 5'
Search 100 bp 3'