Canonical Allele Identifier: CA10576157

Gene: FKBP5

Linked Data

• ClinVar Variation Id: 1702943
• ClinVar RCV Id: RCV003128204
• dbSNP Id: rs4713916
• gnomAD v2: 6-35669983-A-G
• gnomAD v3: 6-35702206-A-G
• gnomAD v4: 6-35702206-A-G
• MyVariant Identifiers: chr6:g.35669983A>G (hg19) ; chr6:g.35702206A>G (hg38)
• PubMed: PMID:15565110 ; PMID:18191112 ; PMID:20709156 ; PMID:22992668

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35702206A>G , CM000668.2:g.35702206A>G	GRCh38
NC_000006.11:g.35669983A>G , CM000668.1:g.35669983A>G	GRCh37
NC_000006.10:g.35777961A>G	NCBI36
NG_012645.2:g.31378T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000536438.5:c.-20+18122T>C	ENSP00000444810.1:n.-20+18122T>C
NM_001145775.2:c.-20+18122T>C	NP_001139247.1:n.-20+18122T>C
NM_001145775.3:c.-20+18122T>C	NP_001139247.1:n.-20+18122T>C