Canonical Allele Identifier: CA2661834653
Gene: PTCHD3P2 HGNC NCBI
KLHL23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169767631T>G , CM000664.2:g.169767631T>G GRCh38
NC_000002.11:g.170624141T>G , CM000664.1:g.170624141T>G GRCh37
NC_000002.10:g.170332387T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000424937.1:n.1087+82A>C (PTCHD3P2)
ENST00000437875.1:c.830-5689T>G (KLHL23) ENSP00000394732.1:n.830-5689T>G
ENST00000448589.1:c.46-8810T>G (KLHL23)