Canonical Allele Identifier: CA2709885381
Gene:

Linked Data

dbSNP Id: rs2112872763

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660992G>C , CM000667.2:g.113660992G>C GRCh38
NC_000005.9:g.112996689G>C , CM000667.1:g.112996689G>C GRCh37
NC_000005.8:g.113024588G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27628G>C