Canonical Allele Identifier: CA448355276
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs2113060407
MyVariant Identifiers: chr5:g.177419979G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992978G>A , CM000667.2:g.177992978G>A GRCh38
NC_000005.9:g.177419979G>A , CM000667.1:g.177419979G>A GRCh37
NC_000005.8:g.177352585G>A NCBI36
NG_015889.1:g.8265C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.412C>T MANE Select ENSP00000311290.2:p.Leu138=
NM_006261.4:c.412C>T NP_006252.3:p.Leu138=
NM_006261.5:c.412C>T MANE Select NP_006252.4:p.Leu138=
Search 100 bp 5'
Search 100 bp 3'