Canonical Allele Identifier: CA64382866
Gene:

Linked Data

dbSNP Id: rs1043084974

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033098G>A , CM000664.2:g.200033098G>A GRCh38
NC_000002.11:g.200897821G>A , CM000664.1:g.200897821G>A GRCh37
NC_000002.10:g.200606066G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22202C>T