Canonical Allele Identifier: CA362378573
Gene: PROP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.177419879T>A (hg19) chr5:g.177992878T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992878T>A , CM000667.2:g.177992878T>A GRCh38
NC_000005.9:g.177419879T>A , CM000667.1:g.177419879T>A GRCh37
NC_000005.8:g.177352485T>A NCBI36
NG_015889.1:g.8365A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.512A>T MANE Select ENSP00000311290.2:p.Tyr171Phe
NM_006261.4:c.512A>T NP_006252.3:p.Tyr171Phe
NM_006261.5:c.512A>T MANE Select NP_006252.4:p.Tyr171Phe
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