Canonical Allele Identifier: CA197059158
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1047014821
gnomAD v3: 9-97852747-G-A
gnomAD v4: 9-97852747-G-A
MyVariant Identifiers: chr9:g.100615029G>A (hg19) chr9:g.97852747G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852747G>A , CM000671.2:g.97852747G>A GRCh38
NC_000009.11:g.100615029G>A , CM000671.1:g.100615029G>A GRCh37
NC_000009.10:g.99654850G>A NCBI36
NG_011979.1:g.4493G>A

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+129C>T
XR_930159.1:n.218+129C>T
XR_930160.1:n.218+129C>T
XR_930161.1:n.218+129C>T
NR_147055.1:n.165+169C>T
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