Canonical Allele Identifier: CA1866690982
Gene: PTCSC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793839_97793842delinsAAAG , CM000671.2:g.97793839_97793842delinsAAAG GRCh38
NC_000009.11:g.100556121_100556124delinsAAAG , CM000671.1:g.100556121_100556124delinsAAAG GRCh37
NC_000009.10:g.99595942_99595945delinsAAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+16053_363+16056delinsCTTT
XR_930162.1:n.6524_6527delinsAAAG
NR_147055.1:n.777+10409_777+10412delinsCTTT
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