Canonical Allele Identifier: CA1541659161
Gene: PLCXD3 HGNC NCBI

Linked Data

dbSNP Id: rs1748267960
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.41475688A>C , CM000667.2:g.41475688A>C GRCh38
NC_000005.9:g.41475790A>C , CM000667.1:g.41475790A>C GRCh37
NC_000005.8:g.41511547A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377801.8:c.103+34736T>G MANE Select ENSP00000367032.3:n.103+34736T>G
ENST00000328457.5:c.103+34736T>G ENSP00000333751.3:n.103+34736T>G
ENST00000377801.7:c.103+34736T>G ENSP00000367032.3:n.103+34736T>G
NM_001005473.2:c.103+34736T>G NP_001005473.1:n.103+34736T>G
NM_001005473.3:c.103+34736T>G MANE Select NP_001005473.1:n.103+34736T>G
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