Canonical Allele Identifier: CA1365145744
Gene:

Linked Data

dbSNP Id: rs1700430004

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53057278C>A , CM000665.2:g.53057278C>A GRCh38
NC_000003.11:g.53091294C>A , CM000665.1:g.53091294C>A GRCh37
NC_000003.10:g.53066334C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-10039G>T
ENST00000607283.5:c.465-14024G>T
ENST00000607495.5:c.447+20410G>T