Canonical Allele Identifier: CA280996468
Gene:

Linked Data

dbSNP Id: rs117471404
MyVariant Identifiers: chr16:g.49108683G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108683G>C , CM000678.2:g.49108683G>C GRCh38
NC_000016.9:g.49142594G>C , CM000678.1:g.49142594G>C GRCh37
NC_000016.8:g.47700095G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1261C>G
XR_001752138.2:n.591+5293C>G
XR_933517.2:n.810+1261C>G