Canonical Allele Identifier: CA3587534
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs760384860
ExAC: 5:177420017 C / T
gnomAD v2: 5-177420017-C-T
gnomAD v3: 5-177993016-C-T
gnomAD v4: 5-177993016-C-T
MyVariant Identifiers: chr5:g.177420017C>T (hg19) chr5:g.177993016C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993016C>T , CM000667.2:g.177993016C>T GRCh38
NC_000005.9:g.177420017C>T , CM000667.1:g.177420017C>T GRCh37
NC_000005.8:g.177352623C>T NCBI36
NG_015889.1:g.8227G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.374G>A MANE Select ENSP00000311290.2:p.Arg125Gln
NM_006261.4:c.374G>A NP_006252.3:p.Arg125Gln
NM_006261.5:c.374G>A MANE Select NP_006252.4:p.Arg125Gln
Search 100 bp 5'
Search 100 bp 3'