Canonical Allele Identifier: CA2718230794
Gene:

Linked Data

dbSNP Id: rs2130167603

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999182A>T , CM000670.2:g.126999182A>T GRCh38
NC_000008.10:g.128011427A>T , CM000670.1:g.128011427A>T GRCh37
NC_000008.9:g.128080609A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1301-7373A>T