Canonical Allele Identifier: CA132896936
Gene: PROP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1810604
ClinVar RCV Id: RCV002510091
dbSNP Id: rs77626899
gnomAD v2: 5-177419590-G-A
gnomAD v3: 5-177992589-G-A
gnomAD v4: 5-177992589-G-A
MyVariant Identifiers: chr5:g.177419590G>A (hg19) chr5:g.177992589G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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