Canonical Allele Identifier: CA1127208660
Gene: PTCSC2 HGNC NCBI

Linked Data

gnomAD v3: 9-97851954-C-A
gnomAD v4: 9-97851954-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851954C>A , CM000671.2:g.97851954C>A GRCh38
NC_000009.11:g.100614236C>A , CM000671.1:g.100614236C>A GRCh37
NC_000009.10:g.99654057C>A NCBI36
NG_011979.1:g.3700C>A

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+922G>T
XR_930159.1:n.218+922G>T
XR_930160.1:n.218+922G>T
XR_930161.1:n.218+922G>T
NR_147055.1:n.165+962G>T