Canonical Allele Identifier: CA1365145736
Gene:

Linked Data

dbSNP Id: rs1700429922

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53057267C>A , CM000665.2:g.53057267C>A GRCh38
NC_000003.11:g.53091283C>A , CM000665.1:g.53091283C>A GRCh37
NC_000003.10:g.53066323C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-10028G>T
ENST00000607283.5:c.465-14013G>T
ENST00000607495.5:c.447+20421G>T