Canonical Allele Identifier: CA2721053069
Gene:

Linked Data

dbSNP Id: rs2132694120

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3375965C>T , CM000672.2:g.3375965C>T GRCh38
NC_000010.10:g.3418157C>T , CM000672.1:g.3418157C>T GRCh37
NC_000010.9:g.3408157C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131187.1:n.162+57109C>T