Canonical Allele Identifier: CA2471091627
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.21318048A= , CM000686.2:g.21318048A= GRCh38
NC_000024.9:g.23479934A= , CM000686.1:g.23479934A= GRCh37
NC_000024.8:g.21889322A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000437359.1:n.752+152A=