Canonical Allele Identifier: CA977566755
Gene:

Linked Data

dbSNP Id: rs1964426284

Genomic Alleles

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

Transcript Alleles

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