Canonical Allele Identifier: CA3587513
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs766265796
ExAC: 5:177419894 C / T
gnomAD v2: 5-177419894-C-T
gnomAD v3: 5-177992893-C-T
gnomAD v4: 5-177992893-C-T
MyVariant Identifiers: chr5:g.177419894C>T (hg19) chr5:g.177992893C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992893C>T , CM000667.2:g.177992893C>T GRCh38
NC_000005.9:g.177419894C>T , CM000667.1:g.177419894C>T GRCh37
NC_000005.8:g.177352500C>T NCBI36
NG_015889.1:g.8350G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.497G>A MANE Select ENSP00000311290.2:p.Cys166Tyr
NM_006261.4:c.497G>A NP_006252.3:p.Cys166Tyr
NM_006261.5:c.497G>A MANE Select NP_006252.4:p.Cys166Tyr
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