Canonical Allele Identifier: CA185688666
Gene:

Linked Data

dbSNP Id: rs181339417

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999523G>C , CM000670.2:g.126999523G>C GRCh38
NC_000008.10:g.128011768G>C , CM000670.1:g.128011768G>C GRCh37
NC_000008.9:g.128080950G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7032G>C