Canonical Allele Identifier: CA1603813937
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1582662774
gnomAD v4: 5-177992700-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992700T>C , CM000667.2:g.177992700T>C GRCh38
NC_000005.9:g.177419701T>C , CM000667.1:g.177419701T>C GRCh37
NC_000005.8:g.177352307T>C NCBI36
NG_015889.1:g.8543A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*9A>G MANE Select ENSP00000311290.2:n.*9A>G
NM_006261.4:c.*9A>G NP_006252.3:n.*9A>G
NM_006261.5:c.*9A>G MANE Select NP_006252.4:n.*9A>G
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