Canonical Allele Identifier: CA1127207951
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1587807013
gnomAD v3: 9-97851889-A-C
gnomAD v4: 9-97851889-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851889A>C , CM000671.2:g.97851889A>C GRCh38
NC_000009.11:g.100614171A>C , CM000671.1:g.100614171A>C GRCh37
NC_000009.10:g.99653992A>C NCBI36
NG_011979.1:g.3635A>C

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+987T>G
XR_930159.1:n.218+987T>G
XR_930160.1:n.218+987T>G
XR_930161.1:n.218+987T>G
NR_147055.1:n.165+1027T>G