Canonical Allele Identifier: CA2060165023
Gene:

Linked Data

dbSNP Id: rs11112046

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.104424414C>G , CM000674.2:g.104424414C>G GRCh38
NC_000012.11:g.104818192C>G , CM000674.1:g.104818192C>G GRCh37
NC_000012.10:g.103342322C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749294.1:n.841-6025C>G
XR_001749295.1:n.1046-6025C>G