Canonical Allele Identifier: CA1866350570
Gene: CTSV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97059329C= , CM000671.2:g.97059329C= GRCh38
NC_000009.11:g.99821611C= , CM000671.1:g.99821611C= GRCh37
NC_000009.10:g.98861432C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000679551.1:n.269+537G=
ENST00000681517.1:n.420+537G=