Canonical Allele Identifier: CA1704517788
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46032971T= , CM000669.2:g.46032971T= GRCh38
NC_000007.13:g.46072569T= , CM000669.1:g.46072569T= GRCh37
NC_000007.12:g.46039094T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745203.1:n.1270-3647T=