Canonical Allele Identifier: CA1320446105
Gene:

Linked Data

dbSNP Id: rs1349867961

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033096A>C , CM000664.2:g.200033096A>C GRCh38
NC_000002.11:g.200897819A>C , CM000664.1:g.200897819A>C GRCh37
NC_000002.10:g.200606064A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22200T>G