Canonical Allele Identifier: CA12829723
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10108511

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11578007T>C , CM000670.2:g.11578007T>C GRCh38
NC_000008.10:g.11435516T>C , CM000670.1:g.11435516T>C GRCh37
NC_000008.9:g.11472925T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-363T>C