Canonical Allele Identifier: CA82727740
Gene: CD86 HGNC NCBI

Linked Data

dbSNP Id: rs995604617
MyVariant Identifiers: chr3:g.122066802A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122066802A>T , CM000665.2:g.122066802A>T GRCh38
NC_000003.11:g.121785649A>T , CM000665.1:g.121785649A>T GRCh37
NC_000003.10:g.123268339A>T NCBI36
NG_029928.1:g.16441A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000330540.7:c.14+11299A>T MANE Select ENSP00000332049.2:n.14+11299A>T
ENST00000330540.6:c.14+11299A>T ENSP00000332049.2:n.14+11299A>T
ENST00000469710.5:c.-183+11299A>T ENSP00000418988.1:n.-183+11299A>T
ENST00000478390.1:n.127+11299A>T
ENST00000493101.5:c.14+11299A>T ENSP00000420230.1:n.14+11299A>T
NM_001206924.1:c.14+11299A>T NP_001193853.1:n.14+11299A>T
NM_001206925.1:c.-183+11299A>T NP_001193854.1:n.-183+11299A>T
NM_175862.4:c.14+11299A>T NP_787058.4:n.14+11299A>T
NM_175862.5:c.14+11299A>T MANE Select NP_787058.5:n.14+11299A>T
NM_001206924.2:c.14+11299A>T NP_001193853.2:n.14+11299A>T
NM_001206925.2:c.-183+11299A>T NP_001193854.2:n.-183+11299A>T