Canonical Allele Identifier: CA994936018
Gene:

Linked Data

dbSNP Id: rs2011164807

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544656T>C , CM000681.2:g.28544656T>C GRCh38
NC_000019.9:g.29035563T>C , CM000681.1:g.29035563T>C GRCh37
NC_000019.8:g.33727403T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77876A>G
XR_243979.1:n.110-51633A>G