Canonical Allele Identifier: CA1365145739
Gene:

Linked Data

dbSNP Id: rs1700429955

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53057274G>A , CM000665.2:g.53057274G>A GRCh38
NC_000003.11:g.53091290G>A , CM000665.1:g.53091290G>A GRCh37
NC_000003.10:g.53066330G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-10035C>T
ENST00000607283.5:c.465-14020C>T
ENST00000607495.5:c.447+20414C>T