Canonical Allele Identifier: CA851854255

Gene: AP3M2

Linked Data

• dbSNP Id: rs1008186299
• gnomAD v3: 8-42169747-A-T
• gnomAD v4: 8-42169747-A-T
• MyVariant Identifiers: chr8:g.42027265A>T (hg19) ; chr8:g.42169747A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42169747A>T , CM000670.2:g.42169747A>T	GRCh38
NC_000008.10:g.42027265A>T , CM000670.1:g.42027265A>T	GRCh37
NC_000008.9:g.42146422A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000396926.8:c.*686A>T MANE Select	ENSP00000380132.3:n.*686A>T
ENST00000174653.3:c.*686A>T	ENSP00000174653.3:n.*686A>T
ENST00000396926.7:c.*686A>T	ENSP00000380132.3:n.*686A>T
ENST00000518421.5:c.*686A>T	ENSP00000428787.1:n.*686A>T
ENST00000520689.1:c.372-142A>T	ENSP00000429804.1:n.372-142A>T
NM_001134296.1:c.*686A>T	NP_001127768.1:n.*686A>T
NM_006803.3:c.*686A>T	NP_006794.1:n.*686A>T
XM_017012977.2:c.*686A>T	XP_016868466.1:n.*686A>T
XR_001745459.2:n.2228A>T
NM_006803.4:c.*686A>T MANE Select	NP_006794.1:n.*686A>T
NM_001134296.2:c.*686A>T	NP_001127768.1:n.*686A>T