Canonical Allele Identifier: CA1127208986
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830602932
gnomAD v3: 9-97852579-G-C
gnomAD v4: 9-97852579-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852579G>C , CM000671.2:g.97852579G>C GRCh38
NC_000009.11:g.100614861G>C , CM000671.1:g.100614861G>C GRCh37
NC_000009.10:g.99654682G>C NCBI36
NG_011979.1:g.4325G>C

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+297C>G
XR_930159.1:n.218+297C>G
XR_930160.1:n.218+297C>G
XR_930161.1:n.218+297C>G
NR_147055.1:n.165+337C>G