Canonical Allele Identifier: CA448346472
Gene: PROP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.177419770G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992769G>C , CM000667.2:g.177992769G>C GRCh38
NC_000005.9:g.177419770G>C , CM000667.1:g.177419770G>C GRCh37
NC_000005.8:g.177352376G>C NCBI36
NG_015889.1:g.8474C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.621C>G MANE Select ENSP00000311290.2:p.Pro207=
NM_006261.4:c.621C>G NP_006252.3:p.Pro207=
NM_006261.5:c.621C>G MANE Select NP_006252.4:p.Pro207=
Search 100 bp 5'
Search 100 bp 3'