Canonical Allele Identifier: CA1118991901
Gene:

Linked Data

dbSNP Id: rs1814938242

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999651A>T , CM000670.2:g.126999651A>T GRCh38
NC_000008.10:g.128011896A>T , CM000670.1:g.128011896A>T GRCh37
NC_000008.9:g.128081078A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6904A>T