Canonical Allele Identifier: CA1502599200
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148649534C= , CM000666.2:g.148649534C= GRCh38
NC_000004.11:g.149570686C= , CM000666.1:g.149570686C= GRCh37
NC_000004.10:g.149790136C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939336.1:n.437-30666G=
XR_001741441.1:n.1745+104950C=
XR_939336.3:n.2921-30666G=