Canonical Allele Identifier: CA2735943391
Gene:

Linked Data

dbSNP Id: rs2122680135

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648218C>T , CM000681.2:g.41648218C>T GRCh38
NC_000019.9:g.42152139C>T , CM000681.1:g.42152139C>T GRCh37
NC_000019.8:g.46843979C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3284G>A