Canonical Allele Identifier: CA362378604
Gene: PROP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.177419892A>T (hg19) chr5:g.177992891A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992891A>T , CM000667.2:g.177992891A>T GRCh38
NC_000005.9:g.177419892A>T , CM000667.1:g.177419892A>T GRCh37
NC_000005.8:g.177352498A>T NCBI36
NG_015889.1:g.8352T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.499T>A MANE Select ENSP00000311290.2:p.Phe167Ile
NM_006261.4:c.499T>A NP_006252.3:p.Phe167Ile
NM_006261.5:c.499T>A MANE Select NP_006252.4:p.Phe167Ile
Search 100 bp 5'
Search 100 bp 3'