Canonical Allele Identifier: CA805180102
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1273363031

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659192A>C , CM000667.2:g.145659192A>C GRCh38
NC_000005.9:g.145038755A>C , CM000667.1:g.145038755A>C GRCh37
NC_000005.8:g.145018948A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105739T>G
XR_944308.1:n.662+105739T>G
XM_017009130.1:c.*6164T>G XP_016864619.1:n.*6164T>G
XM_017009133.1:c.*6196T>G XP_016864622.1:n.*6196T>G
XR_001742025.1:n.913+44783T>G