Canonical Allele Identifier: CA313629721
Gene:

Linked Data

dbSNP Id: rs151184985
MyVariant Identifiers: chr20:g.23661643G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661643G>C , CM000682.2:g.23661643G>C GRCh38
NC_000020.10:g.23642280G>C , CM000682.1:g.23642280G>C GRCh37
NC_000020.9:g.23590280G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.273G>C