Canonical Allele Identifier: CA1563552185
Gene:

Linked Data

dbSNP Id: rs73143387

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222994G>T , CM000667.2:g.92222994G>T GRCh38
NC_000005.9:g.91518811G>T , CM000667.1:g.91518811G>T GRCh37
NC_000005.8:g.91554567G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948565.1:n.394+18310G>T