Canonical Allele Identifier: CA977566751
Gene:

Linked Data

dbSNP Id: rs1964426014

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655547C>T , CM000678.2:g.55655547C>T GRCh38
NC_000016.9:g.55689459C>T , CM000678.1:g.55689459C>T GRCh37
NC_000016.8:g.54246960C>T NCBI36
NG_016969.1:g.4918C>T

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+52G>A