Canonical Allele Identifier: CA129534356
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs183735371
gnomAD v3: 5-145659199-T-C
gnomAD v4: 5-145659199-T-C
MyVariant Identifiers: chr5:g.145038762T>C (hg19) chr5:g.145659199T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145659199T>C , CM000667.2:g.145659199T>C GRCh38
NC_000005.9:g.145038762T>C , CM000667.1:g.145038762T>C GRCh37
NC_000005.8:g.145018955T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.70+105732A>G
XR_944308.1:n.662+105732A>G
XM_017009130.1:c.*6157A>G XP_016864619.1:n.*6157A>G
XM_017009133.1:c.*6189A>G XP_016864622.1:n.*6189A>G
XR_001742025.1:n.913+44776A>G
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