Canonical Allele Identifier: CA2639261560
Gene: ACE HGNC NCBI

Linked Data

gnomAD v4: 17-63483682-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63483682T>C , CM000679.2:g.63483682T>C GRCh38
NC_000017.10:g.61561043T>C , CM000679.1:g.61561043T>C GRCh37
NC_000017.9:g.58914775T>C NCBI36
NG_011648.1:g.11610T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.1586+124T>C MANE Select ENSP00000290866.4:n.1586+124T>C
ENST00000290866.9:c.1586+124T>C ENSP00000290866.4:n.1586+124T>C
ENST00000428043.5:c.1586+124T>C ENSP00000397593.2:n.1586+124T>C
ENST00000582678.5:c.*985+124T>C ENSP00000462995.1:n.*985+124T>C
NM_000789.3:c.1586+124T>C NP_000780.1:n.1586+124T>C
XM_005257110.1:c.1037+124T>C XP_005257167.1:n.1037+124T>C
NM_000789.4:c.1586+124T>C MANE Select NP_000780.1:n.1586+124T>C
NM_001382700.1:c.1019+124T>C NP_001369629.1:n.1019+124T>C
NM_001382701.1:c.734+124T>C NP_001369630.1:n.734+124T>C
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