Canonical Allele Identifier: CA2710761196
Gene:

Linked Data

dbSNP Id: rs1201894982

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943654G>C , CM000668.2:g.11943654G>C GRCh38
NC_000006.11:g.11943887G>C , CM000668.1:g.11943887G>C GRCh37
NC_000006.10:g.12051873G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7881G>C