Canonical Allele Identifier: CA1365145687
Gene:

Linked Data

dbSNP Id: rs1700429112

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53057157A>C , CM000665.2:g.53057157A>C GRCh38
NC_000003.11:g.53091173A>C , CM000665.1:g.53091173A>C GRCh37
NC_000003.10:g.53066213A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9918T>G
ENST00000607283.5:c.465-13903T>G
ENST00000607495.5:c.447+20531T>G