Canonical Allele Identifier: CA1365145572
Gene:

Linked Data

dbSNP Id: rs1700426961

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53056892A>G , CM000665.2:g.53056892A>G GRCh38
NC_000003.11:g.53090908A>G , CM000665.1:g.53090908A>G GRCh37
NC_000003.10:g.53065948A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9653T>C
ENST00000607283.5:c.465-13638T>C
ENST00000607495.5:c.447+20796T>C