Canonical Allele Identifier: CA1603813872
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1772661045
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992559C>G , CM000667.2:g.177992559C>G GRCh38
NC_000005.9:g.177419560C>G , CM000667.1:g.177419560C>G GRCh37
NC_000005.8:g.177352166C>G NCBI36
NG_015889.1:g.8684G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*150G>C MANE Select ENSP00000311290.2:n.*150G>C
NM_006261.4:c.*150G>C NP_006252.3:n.*150G>C
NM_006261.5:c.*150G>C MANE Select NP_006252.4:n.*150G>C
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