Canonical Allele Identifier: CA15440175
Gene: FKBP5 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.35646249T>C
GRCh37 chr6:g.35614026T>C
gnomAD v2:
6:35614026 T / C
gnomAD v3:
6:35646249 T / C
gnomAD v4:
chr6-35646249-T-C
Joint Max Group AF 0.29335642 (AMR)
Genomes Max Group AF 0.29335642 (AMR)
ClinVar RCV:
RCV003128208
ClinVar Variation:
1702947
dbSNP:
4713902
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35646249T>C , CM000668.2:g.35646249T>C GRCh38
NC_000006.11:g.35614026T>C , CM000668.1:g.35614026T>C GRCh37
NC_000006.10:g.35722004T>C NCBI36
NG_012645.2:g.87335A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000357266.9:c.-19-3406A>G MANE Select ENSP00000349811.3:n.-19-3406A>G
ENST00000357266.8:c.-19-3406A>G ENSP00000349811.3:n.-19-3406A>G
ENST00000536438.5:c.-19-3406A>G ENSP00000444810.1:n.-19-3406A>G
ENST00000539068.5:c.-19-3406A>G ENSP00000441205.1:n.-19-3406A>G
ENST00000542713.1:c.-19-3406A>G ENSP00000442340.1:n.-19-3406A>G
NM_001145775.2:c.-19-3406A>G NP_001139247.1:n.-19-3406A>G
NM_001145776.1:c.-19-3406A>G NP_001139248.1:n.-19-3406A>G
NM_001145777.1:c.-19-3406A>G NP_001139249.1:n.-19-3406A>G
NM_004117.3:c.-19-3406A>G NP_004108.1:n.-19-3406A>G
XR_926743.1:n.288-3101T>C
XR_002956345.1:n.1483-3101T>C
NM_001145775.3:c.-19-3406A>G NP_001139247.1:n.-19-3406A>G
NM_001145776.2:c.-19-3406A>G NP_001139248.1:n.-19-3406A>G
NM_001145777.2:c.-19-3406A>G NP_001139249.1:n.-19-3406A>G
NM_004117.4:c.-19-3406A>G MANE Select NP_004108.1:n.-19-3406A>G
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