Canonical Allele Identifier: CA1818149439
Gene:

Linked Data

dbSNP Id: rs1814936128

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999511C>G , CM000670.2:g.126999511C>G GRCh38
NC_000008.10:g.128011756C>G , CM000670.1:g.128011756C>G GRCh37
NC_000008.9:g.128080938C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7044C>G