Canonical Allele Identifier: CA589533009
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1554712865
gnomAD v3: 9-97852062-A-G
gnomAD v4: 9-97852062-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852062A>G , CM000671.2:g.97852062A>G GRCh38
NC_000009.11:g.100614344A>G , CM000671.1:g.100614344A>G GRCh37
NC_000009.10:g.99654165A>G NCBI36
NG_011979.1:g.3808A>G

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+814T>C
XR_930159.1:n.218+814T>C
XR_930160.1:n.218+814T>C
XR_930161.1:n.218+814T>C
NR_147055.1:n.165+854T>C