Canonical Allele Identifier: CA2607210312
Gene:

Linked Data

dbSNP Id: rs2105755278

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033240G>C , CM000664.2:g.200033240G>C GRCh38
NC_000002.11:g.200897963G>C , CM000664.1:g.200897963G>C GRCh37
NC_000002.10:g.200606208G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22344C>G