Canonical Allele Identifier: CA89976958
Gene:

Linked Data

dbSNP Id: rs7653091
gnomAD v3: 3-187931715-C-A
gnomAD v4: 3-187931715-C-A
MyVariant Identifiers: chr3:g.187931715C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187931715C>A , CM000665.2:g.187931715C>A GRCh38
NC_000003.11:g.187649503C>A , CM000665.1:g.187649503C>A GRCh37
NC_000003.10:g.189132197C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924814.1:n.1199G>T
Search 100 bp 5'
Search 100 bp 3'