Canonical Allele Identifier: CA2223789399
Gene:

Linked Data

dbSNP Id: rs1964425514

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655533T>C , CM000678.2:g.55655533T>C GRCh38
NC_000016.9:g.55689445T>C , CM000678.1:g.55689445T>C GRCh37
NC_000016.8:g.54246946T>C NCBI36
NG_016969.1:g.4904T>C

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+66A>G