Canonical Allele Identifier: CA1320446177
Gene:

Linked Data

dbSNP Id: rs1574264589

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033232T>G , CM000664.2:g.200033232T>G GRCh38
NC_000002.11:g.200897955T>G , CM000664.1:g.200897955T>G GRCh37
NC_000002.10:g.200606200T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22336A>C