Canonical Allele Identifier: CA1082548901

Gene: PRELID2

Linked Data

• dbSNP Id: rs1754448132
• gnomAD v3: 5-145659240-T-C
• gnomAD v4: 5-145659240-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.145659240T>C , CM000667.2:g.145659240T>C	GRCh38
NC_000005.9:g.145038803T>C , CM000667.1:g.145038803T>C	GRCh37
NC_000005.8:g.145018996T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000510259.5:n.70+105691A>G
XR_944308.1:n.662+105691A>G
XM_017009130.1:c.*6116A>G	XP_016864619.1:n.*6116A>G
XM_017009133.1:c.*6148A>G	XP_016864622.1:n.*6148A>G
XR_001742025.1:n.913+44735A>G