Canonical Allele Identifier: CA2065107327
Gene:

Linked Data

dbSNP Id: rs1876321920

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398652G>A , CM000674.2:g.115398652G>A GRCh38
NC_000012.11:g.115836457G>A , CM000674.1:g.115836457G>A GRCh37
NC_000012.10:g.114320840G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945389.1:n.697+8443C>T
XR_945389.2:n.701+8443C>T