Canonical Allele Identifier: CA14408025
Gene: ACE3P HGNC NCBI

Linked Data

dbSNP Id: rs8066114
gnomAD v2: 17-61589840-C-G
gnomAD v3: 17-63512479-C-G
gnomAD v4: 17-63512479-C-G
MyVariant Identifiers: chr17:g.61589840C>G (hg19) chr17:g.63512479C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63512479C>G , CM000679.2:g.63512479C>G GRCh38
NC_000017.10:g.61589840C>G , CM000679.1:g.61589840C>G GRCh37
NC_000017.9:g.58943572C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000423435.2:n.1289-903C>G
ENST00000577647.2:c.*1344-903C>G ENSP00000464149.1:n.*1344-903C>G
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