Canonical Allele Identifier: CA10576157
Gene: FKBP5 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.35702206A>G
GRCh37 chr6:g.35669983A>G
gnomAD v2:
6:35669983 A / G
gnomAD v3:
6:35702206 A / G
gnomAD v4:
chr6-35702206-A-G
Joint Max Group AF 0.88905113 (AFR)
Genomes Max Group AF 0.88905113 (AFR)
ClinVar RCV:
RCV003128204
ClinVar Variation:
1702943
dbSNP:
4713916
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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
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