Canonical Allele Identifier: CA805180119
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1430402545

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659238A>C , CM000667.2:g.145659238A>C GRCh38
NC_000005.9:g.145038801A>C , CM000667.1:g.145038801A>C GRCh37
NC_000005.8:g.145018994A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105693T>G
XR_944308.1:n.662+105693T>G
XM_017009130.1:c.*6118T>G XP_016864619.1:n.*6118T>G
XM_017009133.1:c.*6150T>G XP_016864622.1:n.*6150T>G
XR_001742025.1:n.913+44737T>G