Canonical Allele Identifier: CA3624887
Gene: LY86 HGNC NCBI
LY86-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs142081955
gnomAD v2: 6-6588966-C-A
gnomAD v3: 6-6588733-C-A
gnomAD v4: 6-6588733-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6588733C>A , CM000668.2:g.6588733C>A GRCh38
NC_000006.11:g.6588966C>A , CM000668.1:g.6588966C>A GRCh37
NC_000006.10:g.6533965C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230568.5:c.-2C>A (LY86) MANE Select ENSP00000230568.3:n.-2C>A
ENST00000230568.4:c.-2C>A (LY86) ENSP00000230568.3:n.-2C>A
ENST00000379953.6:c.-2C>A (LY86) ENSP00000369286.1:n.-2C>A
NM_004271.3:c.-2C>A (LY86) NP_004262.1:n.-2C>A
NR_026970.1:n.196-19244G>T (LY86-AS1)
XM_017011505.1:c.-2C>A (LY86) XP_016866994.1:n.-2C>A
NM_004271.4:c.-2C>A (LY86) MANE Select NP_004262.1:n.-2C>A