Canonical Allele Identifier: CA211666026
Gene:

Linked Data

dbSNP Id: rs567771831

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762546C>G , CM000672.2:g.94762546C>G GRCh38
NC_000010.10:g.96522303C>G , CM000672.1:g.96522303C>G GRCh37
NC_000010.9:g.96512293C>G NCBI36
NG_008384.2:g.4841C>G
NG_008384.3:g.4866C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12512C>G ENSP00000483243.1:n.932-12512C>G