Canonical Allele Identifier: CA2059285046
Gene:

Linked Data

dbSNP Id: rs1671979477

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501454A>T , CM000674.2:g.102501454A>T GRCh38
NC_000012.11:g.102895232A>T , CM000674.1:g.102895232A>T GRCh37
NC_000012.10:g.101419362A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749289.1:n.1952+17566A>T