Canonical Allele Identifier: CA1603813861
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1772660612
gnomAD v4: 5-177992513-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992513C>T , CM000667.2:g.177992513C>T GRCh38
NC_000005.9:g.177419514C>T , CM000667.1:g.177419514C>T GRCh37
NC_000005.8:g.177352120C>T NCBI36
NG_015889.1:g.8730G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*196G>A MANE Select ENSP00000311290.2:n.*196G>A
NM_006261.4:c.*196G>A NP_006252.3:n.*196G>A
NM_006261.5:c.*196G>A MANE Select NP_006252.4:n.*196G>A
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