Canonical Allele Identifier: CA77246663
Gene:

Linked Data

dbSNP Id: rs918572336
gnomAD v3: 3-72266752-C-T
gnomAD v4: 3-72266752-C-T
MyVariant Identifiers: chr3:g.72315903C>T (hg19) chr3:g.72266752C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266752C>T , CM000665.2:g.72266752C>T GRCh38
NC_000003.11:g.72315903C>T , CM000665.1:g.72315903C>T GRCh37
NC_000003.10:g.72398593C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8356G>A
Search 100 bp 5'
Search 100 bp 3'