Canonical Allele Identifier: CA1127207877
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830589083
gnomAD v3: 9-97851769-C-T
gnomAD v4: 9-97851769-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851769C>T , CM000671.2:g.97851769C>T GRCh38
NC_000009.11:g.100614051C>T , CM000671.1:g.100614051C>T GRCh37
NC_000009.10:g.99653872C>T NCBI36
NG_011979.1:g.3515C>T

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+1107G>A
XR_930159.1:n.218+1107G>A
XR_930160.1:n.218+1107G>A
XR_930161.1:n.218+1107G>A
NR_147055.1:n.165+1147G>A