Canonical Allele Identifier: CA2607136822
Gene:

Linked Data

dbSNP Id: rs2105810596

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195007136T>C , CM000664.2:g.195007136T>C GRCh38
NC_000002.11:g.195871860T>C , CM000664.1:g.195871860T>C GRCh37
NC_000002.10:g.195580105T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739836.1:n.553+52299A>G