Canonical Allele Identifier: CA1866363525
Gene: CTSV HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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