Canonical Allele Identifier: CA77246688
Gene:

Linked Data

dbSNP Id: rs1007030372
MyVariant Identifiers: chr3:g.72316041C>T (hg19) chr3:g.72266890C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266890C>T , CM000665.2:g.72266890C>T GRCh38
NC_000003.11:g.72316041C>T , CM000665.1:g.72316041C>T GRCh37
NC_000003.10:g.72398731C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8218G>A
Search 100 bp 5'
Search 100 bp 3'