Canonical Allele Identifier: CA869019074
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1554712835
MyVariant Identifiers: chr9:g.100614231_100614232insCA (hg19) chr9:g.97851949_97851950insCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851950_97851951insAC , CM000671.2:g.97851950_97851951insAC GRCh38
NC_000009.11:g.100614232_100614233insAC , CM000671.1:g.100614232_100614233insAC GRCh37
NC_000009.10:g.99654053_99654054insAC NCBI36
NG_011979.1:g.3696_3697insAC

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+926_218+927insTG
XR_930159.1:n.218+926_218+927insTG
XR_930160.1:n.218+926_218+927insTG
XR_930161.1:n.218+926_218+927insTG
NR_147055.1:n.165+966_165+967insTG
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