Canonical Allele Identifier: CA211666011
Gene:

Linked Data

dbSNP Id: rs547923030

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762537T>G , CM000672.2:g.94762537T>G GRCh38
NC_000010.10:g.96522294T>G , CM000672.1:g.96522294T>G GRCh37
NC_000010.9:g.96512284T>G NCBI36
NG_008384.2:g.4832T>G
NG_008384.3:g.4857T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12521T>G ENSP00000483243.1:n.932-12521T>G