Canonical Allele Identifier: CA132897332
Gene: PROP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2873133
ClinVar RCV Id: RCV003709712
dbSNP Id: rs933972141
MyVariant Identifiers: chr5:g.177419965G>A (hg19) chr5:g.177992964G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992964G>A , CM000667.2:g.177992964G>A GRCh38
NC_000005.9:g.177419965G>A , CM000667.1:g.177419965G>A GRCh37
NC_000005.8:g.177352571G>A NCBI36
NG_015889.1:g.8279C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.426C>T MANE Select ENSP00000311290.2:p.Ala142=
NM_006261.4:c.426C>T NP_006252.3:p.Ala142=
NM_006261.5:c.426C>T MANE Select NP_006252.4:p.Ala142=
Search 100 bp 5'
Search 100 bp 3'