Canonical Allele Identifier: CA1284436071
Gene:

Linked Data

dbSNP Id: rs1679097481

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122379220G>C , CM000664.2:g.122379220G>C GRCh38
NC_000002.11:g.123136796G>C , CM000664.1:g.123136796G>C GRCh37
NC_000002.10:g.122853266G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-13743G>C
XR_001739684.1:n.556-13743G>C