Canonical Allele Identifier: CA2047190525
Gene:

Linked Data

dbSNP Id: rs1177092539

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004990G>C , CM000674.2:g.76004990G>C GRCh38
NC_000012.11:g.76398770G>C , CM000674.1:g.76398770G>C GRCh37
NC_000012.10:g.74685037G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945110.1:n.311+1199C>G
XR_001749218.2:n.402+1199C>G
XR_945110.3:n.402+1199C>G