Canonical Allele Identifier: CA1804794142
Gene:

Linked Data

dbSNP Id: rs891115171

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269578G>C , CM000670.2:g.97269578G>C GRCh38
NC_000008.10:g.98281806G>C , CM000670.1:g.98281806G>C GRCh37
NC_000008.9:g.98350982G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149492C>G