Canonical Allele Identifier: CA2223789413
Gene:

Linked Data

dbSNP Id: rs1964426284

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655564C>A , CM000678.2:g.55655564C>A GRCh38
NC_000016.9:g.55689476C>A , CM000678.1:g.55689476C>A GRCh37
NC_000016.8:g.54246977C>A NCBI36
NG_016969.1:g.4935C>A

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+35G>T