Canonical Allele Identifier: CA984456414
Gene:

Linked Data

dbSNP Id: rs1908569805

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211749C>G , CM000679.2:g.50211749C>G GRCh38
NC_000017.10:g.48289110C>G , CM000679.1:g.48289110C>G GRCh37
NC_000017.9:g.45644109C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-2086C>G