Canonical Allele Identifier: CA197059071
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs995785198
gnomAD v2: 9-100614316-A-G
gnomAD v3: 9-97852034-A-G
gnomAD v4: 9-97852034-A-G
MyVariant Identifiers: chr9:g.100614316A>G (hg19) chr9:g.97852034A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852034A>G , CM000671.2:g.97852034A>G GRCh38
NC_000009.11:g.100614316A>G , CM000671.1:g.100614316A>G GRCh37
NC_000009.10:g.99654137A>G NCBI36
NG_011979.1:g.3780A>G

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+842T>C
XR_930159.1:n.218+842T>C
XR_930160.1:n.218+842T>C
XR_930161.1:n.218+842T>C
NR_147055.1:n.165+882T>C
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