Canonical Allele Identifier: CA1804794419
Gene:

Linked Data

dbSNP Id: rs937535309

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269770G>C , CM000670.2:g.97269770G>C GRCh38
NC_000008.10:g.98281998G>C , CM000670.1:g.98281998G>C GRCh37
NC_000008.9:g.98351174G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149300C>G