Canonical Allele Identifier: CA211665955
Gene:

Linked Data

dbSNP Id: rs1027788763

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762471A>G , CM000672.2:g.94762471A>G GRCh38
NC_000010.10:g.96522228A>G , CM000672.1:g.96522228A>G GRCh37
NC_000010.9:g.96512218A>G NCBI36
NG_008384.2:g.4766A>G
NG_008384.3:g.4791A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12587A>G ENSP00000483243.1:n.932-12587A>G