Canonical Allele Identifier: CA71252399
Gene:

Linked Data

dbSNP Id: rs994401573
MyVariant Identifiers: chr3:g.21248569T>C (hg19) chr3:g.21207077T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21207077T>C , CM000665.2:g.21207077T>C GRCh38
NC_000003.11:g.21248569T>C , CM000665.1:g.21248569T>C GRCh37
NC_000003.10:g.21223573T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940646.1:n.254-3921T>C
XR_940646.2:n.547-3921T>C
Search 100 bp 5'
Search 100 bp 3'