Canonical Allele Identifier: CA1649525024
Gene:

Linked Data

dbSNP Id: rs901630

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98091643C>A , CM000668.2:g.98091643C>A GRCh38
NC_000006.11:g.98539519C>A , CM000668.1:g.98539519C>A GRCh37
NC_000006.10:g.98646240C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.372-7543C>A
XR_942809.1:n.372-7543C>A