Canonical Allele Identifier: CA3624888
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs750844218
ExAC: 6:6588969 T / C
gnomAD v2: 6-6588969-T-C
gnomAD v4: 6-6588736-T-C
MyVariant Identifiers: chr6:g.6588969T>C (hg19) chr6:g.6588736T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588736T>C , CM000668.2:g.6588736T>C GRCh38
NC_000006.11:g.6588969T>C , CM000668.1:g.6588969T>C GRCh37
NC_000006.10:g.6533968T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.2T>C (LY86) MANE Select ENSP00000230568.3:p.Met1Thr
ENST00000230568.4:c.2T>C (LY86) ENSP00000230568.3:p.Met1Thr
ENST00000379953.6:c.2T>C (LY86) ENSP00000369286.1:p.Met1Thr
NM_004271.3:c.2T>C (LY86) NP_004262.1:p.Met1Thr
NR_026970.1:n.196-19247A>G (LY86-AS1)
XM_017011505.1:c.2T>C (LY86) XP_016866994.1:p.Met1Thr
NM_004271.4:c.2T>C (LY86) MANE Select NP_004262.1:p.Met1Thr
Search 100 bp 5'
Search 100 bp 3'