Canonical Allele Identifier: CA1084892797
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1772661540
gnomAD v4: 5-177992585-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992585A>G , CM000667.2:g.177992585A>G GRCh38
NC_000005.9:g.177419586A>G , CM000667.1:g.177419586A>G GRCh37
NC_000005.8:g.177352192A>G NCBI36
NG_015889.1:g.8658T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*124T>C MANE Select ENSP00000311290.2:n.*124T>C
NM_006261.4:c.*124T>C NP_006252.3:n.*124T>C
NM_006261.5:c.*124T>C MANE Select NP_006252.4:n.*124T>C
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