Canonical Allele Identifier: CA2059285051
Gene:

Linked Data

dbSNP Id: rs1881755495

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501467G>T , CM000674.2:g.102501467G>T GRCh38
NC_000012.11:g.102895245G>T , CM000674.1:g.102895245G>T GRCh37
NC_000012.10:g.101419375G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17579G>T