Canonical Allele Identifier: CA869018779
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1291633383
gnomAD v3: 9-97851842-G-T
gnomAD v4: 9-97851842-G-T
MyVariant Identifiers: chr9:g.100614124G>T (hg19) chr9:g.97851842G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851842G>T , CM000671.2:g.97851842G>T GRCh38
NC_000009.11:g.100614124G>T , CM000671.1:g.100614124G>T GRCh37
NC_000009.10:g.99653945G>T NCBI36
NG_011979.1:g.3588G>T

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+1034C>A
XR_930159.1:n.218+1034C>A
XR_930160.1:n.218+1034C>A
XR_930161.1:n.218+1034C>A
NR_147055.1:n.165+1074C>A
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