Canonical Allele Identifier: CA1603813889
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs77626899
gnomAD v4: 5-177992589-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992589G>T , CM000667.2:g.177992589G>T GRCh38
NC_000005.9:g.177419590G>T , CM000667.1:g.177419590G>T GRCh37
NC_000005.8:g.177352196G>T NCBI36
NG_015889.1:g.8654C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*120C>A MANE Select ENSP00000311290.2:n.*120C>A
NM_006261.4:c.*120C>A NP_006252.3:n.*120C>A
NM_006261.5:c.*120C>A MANE Select NP_006252.4:n.*120C>A
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