Canonical Allele Identifier: CA892581797
Gene:

Linked Data

dbSNP Id: rs1252819297
gnomAD v3: 2-70438447-T-G
gnomAD v4: 2-70438447-T-G
MyVariant Identifiers: chr2:g.70438447T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70438447T>G , CM000664.2:g.70438447T>G GRCh38
NC_000002.11:g.70665579T>G , CM000664.1:g.70665579T>G GRCh37
NC_000002.10:g.70519087T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940229.1:n.230-2853T>G