Canonical Allele Identifier: CA16055246
Gene: DOCK7 HGNC NCBI

Linked Data

dbSNP Id: rs636523
gnomAD v2: 1-62920008-A-G
gnomAD v3: 1-62454337-A-G
gnomAD v4: 1-62454337-A-G
MyVariant Identifiers: chr1:g.62920008A>G (hg19) chr1:g.62454337A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62454337A>G , CM000663.2:g.62454337A>G GRCh38
NC_000001.10:g.62920008A>G , CM000663.1:g.62920008A>G GRCh37
NC_000001.9:g.62692596A>G NCBI36
NG_033073.1:g.239032T>C
NG_033073.2:g.239032T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000634495.2:n.3639T>C
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