Canonical Allele Identifier: CA1438691231
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.11628425T= , CM000666.2:g.11628425T= GRCh38
NC_000004.11:g.11630049T= , CM000666.1:g.11630049T= GRCh37
NC_000004.10:g.11239147T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741361.1:n.1026+76471T=