Canonical Allele Identifier: CA869019659

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1367730032
• gnomAD v3: 9-97852822-A-T
• gnomAD v4: 9-97852822-A-T
• MyVariant Identifiers: chr9:g.100615104A>T (hg19) ; chr9:g.97852822A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97852822A>T , CM000671.2:g.97852822A>T	GRCh38
NC_000009.11:g.100615104A>T , CM000671.1:g.100615104A>T	GRCh37
NC_000009.10:g.99654925A>T	NCBI36
NG_011979.1:g.4568A>T

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+54T>A
XR_930159.1:n.218+54T>A
XR_930160.1:n.218+54T>A
XR_930161.1:n.218+54T>A
NR_147055.1:n.165+94T>A