Canonical Allele Identifier: CA607929856
Gene: HPD HGNC NCBI

Linked Data

dbSNP Id: rs1469527364
gnomAD v2: 12-122284843-G-C
gnomAD v4: 12-121846937-G-C
MyVariant Identifiers: chr12:g.122284843G>C (hg19) chr12:g.121846937G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121846937G>C , CM000674.2:g.121846937G>C GRCh38
NC_000012.11:g.122284843G>C , CM000674.1:g.122284843G>C GRCh37
NC_000012.10:g.120769226G>C NCBI36
NG_016461.1:g.46675C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289004.8:c.760-4C>G MANE Select ENSP00000289004.4:n.760-4C>G
ENST00000543163.5:c.643-4C>G ENSP00000441677.1:n.643-4C>G
NM_001171993.1:c.643-4C>G NP_001165464.1:n.643-4C>G
NM_002150.2:c.760-4C>G NP_002141.1:n.760-4C>G
NM_002150.3:c.760-4C>G MANE Select NP_002141.2:n.760-4C>G
NM_001171993.2:c.643-4C>G NP_001165464.1:n.643-4C>G
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