Canonical Allele Identifier: CA1866363524
Gene: CTSV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97069874C= , CM000671.2:g.97069874C= GRCh38
NC_000009.11:g.99832156C= , CM000671.1:g.99832156C= GRCh37
NC_000009.10:g.98871977C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000679551.1:n.164-9903G=
ENST00000681517.1:n.315-9903G=