Canonical Allele Identifier: CA188145872
Gene:

Linked Data

dbSNP Id: rs183229601
gnomAD v2: 9-1787611-A-T
gnomAD v3: 9-1787611-A-T
gnomAD v4: 9-1787611-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787611A>T , CM000671.2:g.1787611A>T GRCh38
NC_000009.11:g.1787611A>T , CM000671.1:g.1787611A>T GRCh37
NC_000009.10:g.1777611A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746599.1:n.142+68699A>T