Canonical Allele Identifier: CA2336566001
Gene:

Linked Data

dbSNP Id: rs2071922901

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648250G>A , CM000681.2:g.41648250G>A GRCh38
NC_000019.9:g.42152171G>A , CM000681.1:g.42152171G>A GRCh37
NC_000019.8:g.46844011G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3252C>T