Canonical Allele Identifier: CA909861232
Gene:

Linked Data

dbSNP Id: rs1487497590
MyVariant Identifiers: chr3:g.70626269C>T (hg19) chr3:g.70577118C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577118C>T , CM000665.2:g.70577118C>T GRCh38
NC_000003.11:g.70626269C>T , CM000665.1:g.70626269C>T GRCh37
NC_000003.10:g.70708959C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940947.1:n.407-1165G>A
XR_001740559.1:n.367-1165G>A
Search 100 bp 5'
Search 100 bp 3'