Canonical Allele Identifier: CA2750386032
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70438486T>C , CM000664.2:g.70438486T>C GRCh38
NC_000002.11:g.70665618T>C , CM000664.1:g.70665618T>C GRCh37
NC_000002.10:g.70519126T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940229.1:n.230-2814T>C