Canonical Allele Identifier: CA2838516735
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3679681T>C , CM000672.2:g.3679681T>C GRCh38
NC_000010.10:g.3721873T>C , CM000672.1:g.3721873T>C GRCh37
NC_000010.9:g.3711873T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131187.1:n.163-69007T>C