Canonical Allele Identifier: CA586058576
Gene:

Linked Data

dbSNP Id: rs1231797645
gnomAD v2: 9-1787379-A-C
gnomAD v3: 9-1787379-A-C
gnomAD v4: 9-1787379-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787379A>C , CM000671.2:g.1787379A>C GRCh38
NC_000009.11:g.1787379A>C , CM000671.1:g.1787379A>C GRCh37
NC_000009.10:g.1777379A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68467A>C