Canonical Allele Identifier: CA857362195
Gene:

Linked Data

dbSNP Id: rs1322696396

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269645T>C , CM000670.2:g.97269645T>C GRCh38
NC_000008.10:g.98281873T>C , CM000670.1:g.98281873T>C GRCh37
NC_000008.9:g.98351049T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149425A>G