Canonical Allele Identifier: CA2391130619
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43168902G= , CM000683.2:g.43168902G= GRCh38
NG_009823.1:g.4872G=

Transcript Alleles

HGVS Amino-acid Change
XR_001755073.1:n.647+2135C=