Canonical Allele Identifier: CA721927973
Gene:

Linked Data

dbSNP Id: rs1318531227

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655565C>T , CM000678.2:g.55655565C>T GRCh38
NC_000016.9:g.55689477C>T , CM000678.1:g.55689477C>T GRCh37
NC_000016.8:g.54246978C>T NCBI36
NG_016969.1:g.4936C>T

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+34G>A