Canonical Allele Identifier: CA2605142680
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs2149675924

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659172T>C , CM000667.2:g.145659172T>C GRCh38
NC_000005.9:g.145038735T>C , CM000667.1:g.145038735T>C GRCh37
NC_000005.8:g.145018928T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105759A>G
XR_944308.1:n.662+105759A>G
XM_017009130.1:c.*6184A>G XP_016864619.1:n.*6184A>G
XM_017009133.1:c.*6216A>G XP_016864622.1:n.*6216A>G
XR_001742025.1:n.913+44803A>G