Canonical Allele Identifier: CA1804794109
Gene:

Linked Data

dbSNP Id: rs888003681

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269557G>T , CM000670.2:g.97269557G>T GRCh38
NC_000008.10:g.98281785G>T , CM000670.1:g.98281785G>T GRCh37
NC_000008.9:g.98350961G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149513C>A