Canonical Allele Identifier: CA1118991862
Gene:

Linked Data

dbSNP Id: rs994091299

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999518C>G , CM000670.2:g.126999518C>G GRCh38
NC_000008.10:g.128011763C>G , CM000670.1:g.128011763C>G GRCh37
NC_000008.9:g.128080945C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7037C>G