Canonical Allele Identifier: CA808118026
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs375043120
MyVariant Identifiers: chr5:g.177420266G>C (hg19) chr5:g.177993265G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993265G>C , CM000667.2:g.177993265G>C GRCh38
NC_000005.9:g.177420266G>C , CM000667.1:g.177420266G>C GRCh37
NC_000005.8:g.177352872G>C NCBI36
NG_015889.1:g.7978C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.343-218C>G MANE Select ENSP00000311290.2:n.343-218C>G
NM_006261.4:c.343-218C>G NP_006252.3:n.343-218C>G
NM_006261.5:c.343-218C>G MANE Select NP_006252.4:n.343-218C>G
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