Canonical Allele Identifier: CA1438624487
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.11501904C= , CM000666.2:g.11501904C= GRCh38
NC_000004.11:g.11503528C= , CM000666.1:g.11503528C= GRCh37
NC_000004.10:g.11112626C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741361.1:n.950+19058C=