Canonical Allele Identifier: CA896967387
Gene:

Linked Data

dbSNP Id: rs1384806158

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743557G>T , CM000665.2:g.109743557G>T GRCh38
NC_000003.11:g.109462404G>T , CM000665.1:g.109462404G>T GRCh37
NC_000003.10:g.110945094G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924325.1:n.142+63362G>T