Canonical Allele Identifier: CA756180396
Gene:

Linked Data

dbSNP Id: rs1248390462

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122379261G>C , CM000664.2:g.122379261G>C GRCh38
NC_000002.11:g.123136837G>C , CM000664.1:g.123136837G>C GRCh37
NC_000002.10:g.122853307G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-13702G>C
XR_001739684.1:n.556-13702G>C