Canonical Allele Identifier: CA2838485206
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.131854178T>G , CM000669.2:g.131854178T>G GRCh38
NC_000007.13:g.131538937T>G , CM000669.1:g.131538937T>G GRCh37
NC_000007.12:g.131189477T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745363.1:n.219+8900T>G