Canonical Allele Identifier: CA2491383603
Gene:

Linked Data

dbSNP Id: rs755670820

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458187G>T , CM000664.2:g.16458187G>T GRCh38
NC_000002.11:g.16639455G>T , CM000664.1:g.16639455G>T GRCh37
NC_000002.10:g.16502936G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939752.1:n.396-3093C>A