Canonical Allele Identifier: CA1127207852
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830588704

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851734A>G , CM000671.2:g.97851734A>G GRCh38
NC_000009.11:g.100614016A>G , CM000671.1:g.100614016A>G GRCh37
NC_000009.10:g.99653837A>G NCBI36
NG_011979.1:g.3480A>G

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+1142T>C
XR_930159.1:n.218+1142T>C
XR_930160.1:n.218+1142T>C
XR_930161.1:n.218+1142T>C
NR_147055.1:n.165+1182T>C