Canonical Allele Identifier: CA1365145588
Gene:

Linked Data

dbSNP Id: rs1700427294

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53056940A>G , CM000665.2:g.53056940A>G GRCh38
NC_000003.11:g.53090956A>G , CM000665.1:g.53090956A>G GRCh37
NC_000003.10:g.53065996A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9701T>C
ENST00000607283.5:c.465-13686T>C
ENST00000607495.5:c.447+20748T>C