Canonical Allele Identifier: CA362379432
Gene: PROP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.177422834G>T (hg19) chr5:g.177995833G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995833G>T , CM000667.2:g.177995833G>T GRCh38
NC_000005.9:g.177422834G>T , CM000667.1:g.177422834G>T GRCh37
NC_000005.8:g.177355440G>T NCBI36
NG_015889.1:g.5410C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.101C>A MANE Select ENSP00000311290.2:p.Thr34Asn
NM_006261.4:c.101C>A NP_006252.3:p.Thr34Asn
NM_006261.5:c.101C>A MANE Select NP_006252.4:p.Thr34Asn
Search 100 bp 5'
Search 100 bp 3'