Canonical Allele Identifier: CA2701396441
Gene:

Linked Data

dbSNP Id: rs2105755198

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033045T>C , CM000664.2:g.200033045T>C GRCh38
NC_000002.11:g.200897768T>C , CM000664.1:g.200897768T>C GRCh37
NC_000002.10:g.200606013T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22149A>G