Canonical Allele Identifier: CA65737701
Gene:

Linked Data

dbSNP Id: rs781575332

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216605G>C , CM000664.2:g.218216605G>C GRCh38
NC_000002.11:g.219081328G>C , CM000664.1:g.219081328G>C GRCh37
NC_000002.10:g.218789573G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241416.2:n.340C>G
XR_923908.1:n.337C>G