Canonical Allele Identifier: CA545642796
Gene: CD86 HGNC NCBI

Linked Data

dbSNP Id: rs1227856361
gnomAD v2: 3-121785602-T-A
gnomAD v3: 3-122066755-T-A
gnomAD v4: 3-122066755-T-A
MyVariant Identifiers: chr3:g.121785602T>A (hg19) chr3:g.122066755T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122066755T>A , CM000665.2:g.122066755T>A GRCh38
NC_000003.11:g.121785602T>A , CM000665.1:g.121785602T>A GRCh37
NC_000003.10:g.123268292T>A NCBI36
NG_029928.1:g.16394T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000330540.7:c.14+11252T>A MANE Select ENSP00000332049.2:n.14+11252T>A
ENST00000330540.6:c.14+11252T>A ENSP00000332049.2:n.14+11252T>A
ENST00000469710.5:c.-183+11252T>A ENSP00000418988.1:n.-183+11252T>A
ENST00000478390.1:n.127+11252T>A
ENST00000493101.5:c.14+11252T>A ENSP00000420230.1:n.14+11252T>A
NM_001206924.1:c.14+11252T>A NP_001193853.1:n.14+11252T>A
NM_001206925.1:c.-183+11252T>A NP_001193854.1:n.-183+11252T>A
NM_175862.4:c.14+11252T>A NP_787058.4:n.14+11252T>A
NM_175862.5:c.14+11252T>A MANE Select NP_787058.5:n.14+11252T>A
NM_001206924.2:c.14+11252T>A NP_001193853.2:n.14+11252T>A
NM_001206925.2:c.-183+11252T>A NP_001193854.2:n.-183+11252T>A
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