Canonical Allele Identifier: CA3587639
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs144314831
ExAC: 5:177422839 C / A
gnomAD v2: 5-177422839-C-A
gnomAD v4: 5-177995838-C-A
MyVariant Identifiers: chr5:g.177422839C>A (hg19) chr5:g.177995838C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995838C>A , CM000667.2:g.177995838C>A GRCh38
NC_000005.9:g.177422839C>A , CM000667.1:g.177422839C>A GRCh37
NC_000005.8:g.177355445C>A NCBI36
NG_015889.1:g.5405G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.96G>T MANE Select ENSP00000311290.2:p.Pro32=
NM_006261.4:c.96G>T NP_006252.3:p.Pro32=
NM_006261.5:c.96G>T MANE Select NP_006252.4:p.Pro32=
Search 100 bp 5'
Search 100 bp 3'