Canonical Allele Identifier: CA827168780
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1422217275
gnomAD v3: 6-6610292-T-C
gnomAD v4: 6-6610292-T-C
MyVariant Identifiers: chr6:g.6610525T>C (hg19) chr6:g.6610292T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6610292T>C , CM000668.2:g.6610292T>C GRCh38
NC_000006.11:g.6610525T>C , CM000668.1:g.6610525T>C GRCh37
NC_000006.10:g.6555524T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000230568.5:c.137-14634T>C (LY86) MANE Select ENSP00000230568.3:n.137-14634T>C
ENST00000230568.4:c.137-14634T>C (LY86) ENSP00000230568.3:n.137-14634T>C
ENST00000379953.6:c.137-14634T>C (LY86) ENSP00000369286.1:n.137-14634T>C
NM_004271.3:c.137-14634T>C (LY86) NP_004262.1:n.137-14634T>C
NR_026970.1:n.195+12340A>G (LY86-AS1)
XM_017011505.1:c.137-14634T>C (LY86) XP_016866994.1:n.137-14634T>C
NM_004271.4:c.137-14634T>C (LY86) MANE Select NP_004262.1:n.137-14634T>C
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