Canonical Allele Identifier: CA2698684546
Gene:

Linked Data

dbSNP Id: rs2103349946

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458177C>T , CM000664.2:g.16458177C>T GRCh38
NC_000002.11:g.16639445C>T , CM000664.1:g.16639445C>T GRCh37
NC_000002.10:g.16502926C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3083G>A