Canonical Allele Identifier: CA1827744341
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787611A= , CM000671.2:g.1787611A= GRCh38
NC_000009.11:g.1787611A= , CM000671.1:g.1787611A= GRCh37
NC_000009.10:g.1777611A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746599.1:n.142+68699A=