Canonical Allele Identifier: CA1502599601
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148649669T= , CM000666.2:g.148649669T= GRCh38
NC_000004.11:g.149570821T= , CM000666.1:g.149570821T= GRCh37
NC_000004.10:g.149790271T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939336.1:n.436+30663A=
XR_001741441.1:n.1745+105085T=
XR_939336.3:n.2920+30663A=