Canonical Allele Identifier: CA915796443
Gene: PTCSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851949_97851950insTCCC , CM000671.2:g.97851949_97851950insTCCC GRCh38
NC_000009.11:g.100614231_100614232insTCCC , CM000671.1:g.100614231_100614232insTCCC GRCh37
NC_000009.10:g.99654052_99654053insTCCC NCBI36
NG_011979.1:g.3695_3696insTCCC

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+929_218+930insAGGG
XR_930159.1:n.218+929_218+930insAGGG
XR_930160.1:n.218+929_218+930insAGGG
XR_930161.1:n.218+929_218+930insAGGG
NR_147055.1:n.165+969_165+970insAGGG