Canonical Allele Identifier: CA1365145738
Gene:

Linked Data

dbSNP Id: rs1700429939

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53057268A>G , CM000665.2:g.53057268A>G GRCh38
NC_000003.11:g.53091284A>G , CM000665.1:g.53091284A>G GRCh37
NC_000003.10:g.53066324A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-10029T>C
ENST00000607283.5:c.465-14014T>C
ENST00000607495.5:c.447+20420T>C