Canonical Allele Identifier: CA197059073
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs951139244
gnomAD v3: 9-97852050-C-T
gnomAD v4: 9-97852050-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852050C>T , CM000671.2:g.97852050C>T GRCh38
NC_000009.11:g.100614332C>T , CM000671.1:g.100614332C>T GRCh37
NC_000009.10:g.99654153C>T NCBI36
NG_011979.1:g.3796C>T

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+826G>A
XR_930159.1:n.218+826G>A
XR_930160.1:n.218+826G>A
XR_930161.1:n.218+826G>A
NR_147055.1:n.165+866G>A