Canonical Allele Identifier: CA2676774069
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992593-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992593A>G , CM000667.2:g.177992593A>G GRCh38
NC_000005.9:g.177419594A>G , CM000667.1:g.177419594A>G GRCh37
NC_000005.8:g.177352200A>G NCBI36
NG_015889.1:g.8650T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*116T>C MANE Select ENSP00000311290.2:n.*116T>C
NM_006261.4:c.*116T>C NP_006252.3:n.*116T>C
NM_006261.5:c.*116T>C MANE Select NP_006252.4:n.*116T>C
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