Canonical Allele Identifier: CA207989743
Gene:

Linked Data

dbSNP Id: rs973480599

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812986T>C , CM000672.2:g.57812986T>C GRCh38
NC_000010.10:g.59572746T>C , CM000672.1:g.59572746T>C GRCh37
NC_000010.9:g.59242752T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34306A>G
XR_001747454.1:n.85+34306A>G