Canonical Allele Identifier: CA2491383693
Gene:

Linked Data

dbSNP Id: rs1664554338

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458378A>C , CM000664.2:g.16458378A>C GRCh38
NC_000002.11:g.16639646A>C , CM000664.1:g.16639646A>C GRCh37
NC_000002.10:g.16503127A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3284T>G