Canonical Allele Identifier: CA869018701
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1279108611
gnomAD v3: 9-97851676-C-T
gnomAD v4: 9-97851676-C-T
MyVariant Identifiers: chr9:g.100613958C>T (hg19) chr9:g.97851676C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851676C>T , CM000671.2:g.97851676C>T GRCh38
NC_000009.11:g.100613958C>T , CM000671.1:g.100613958C>T GRCh37
NC_000009.10:g.99653779C>T NCBI36
NG_011979.1:g.3422C>T

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+1200G>A
XR_930159.1:n.218+1200G>A
XR_930160.1:n.218+1200G>A
XR_930161.1:n.218+1200G>A
NR_147055.1:n.165+1240G>A
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