Canonical Allele Identifier: CA824228087

Gene: FKBP5

Linked Data

• dbSNP Id: rs7757037
• gnomAD v3: 6-35580459-G-T
• gnomAD v4: 6-35580459-G-T
• MyVariant Identifiers: chr6:g.35548236G>T (hg19) ; chr6:g.35580459G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35580459G>T , CM000668.2:g.35580459G>T	GRCh38
NC_000006.11:g.35548236G>T , CM000668.1:g.35548236G>T	GRCh37
NC_000006.10:g.35656214G>T	NCBI36
NG_012645.2:g.153125C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357266.9:c.841-238C>A MANE Select	ENSP00000349811.3:n.841-238C>A
ENST00000357266.8:c.841-238C>A	ENSP00000349811.3:n.841-238C>A
ENST00000536438.5:c.841-238C>A	ENSP00000444810.1:n.841-238C>A
ENST00000539068.5:c.841-238C>A	ENSP00000441205.1:n.841-238C>A
NM_001145775.2:c.841-238C>A	NP_001139247.1:n.841-238C>A
NM_001145776.1:c.841-238C>A	NP_001139248.1:n.841-238C>A
NM_004117.3:c.841-238C>A	NP_004108.1:n.841-238C>A
XR_242006.2:n.433-12571G>T
XR_242006.3:n.462-12571G>T
NM_001145775.3:c.841-238C>A	NP_001139247.1:n.841-238C>A
NM_001145776.2:c.841-238C>A	NP_001139248.1:n.841-238C>A
NM_004117.4:c.841-238C>A MANE Select	NP_004108.1:n.841-238C>A