Canonical Allele Identifier: CA2698772066
Gene:

Linked Data

dbSNP Id: rs765845990

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17843936C>G , CM000664.2:g.17843936C>G GRCh38
NC_000002.11:g.18025203C>G , CM000664.1:g.18025203C>G GRCh37
NC_000002.10:g.17888684C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3758G>C