Canonical Allele Identifier: CA1127208862
Gene: PTCSC2 HGNC NCBI

Linked Data

gnomAD v3: 9-97852304-A-C
gnomAD v4: 9-97852304-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852304A>C , CM000671.2:g.97852304A>C GRCh38
NC_000009.11:g.100614586A>C , CM000671.1:g.100614586A>C GRCh37
NC_000009.10:g.99654407A>C NCBI36
NG_011979.1:g.4050A>C

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+572T>G
XR_930159.1:n.218+572T>G
XR_930160.1:n.218+572T>G
XR_930161.1:n.218+572T>G
NR_147055.1:n.165+612T>G