Canonical Allele Identifier: CA1728106774
Gene:

Linked Data

dbSNP Id: rs1789258339

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388590G>T , CM000669.2:g.97388590G>T GRCh38
NC_000007.13:g.97017902G>T , CM000669.1:g.97017902G>T GRCh37
NC_000007.12:g.96855838G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59943C>A