Canonical Allele Identifier: CA619976110
Gene:

Linked Data

dbSNP Id: rs1316837980

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782364A>G , CM000677.2:g.95782364A>G GRCh38
NC_000015.9:g.96325593A>G , CM000677.1:g.96325593A>G GRCh37
NC_000015.8:g.94126597A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42825A>G