Canonical Allele Identifier: CA448346436
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v3: 5-177992727-T-G
gnomAD v4: 5-177992727-T-G
MyVariant Identifiers: chr5:g.177419728T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992727T>G , CM000667.2:g.177992727T>G GRCh38
NC_000005.9:g.177419728T>G , CM000667.1:g.177419728T>G GRCh37
NC_000005.8:g.177352334T>G NCBI36
NG_015889.1:g.8516A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.663A>C MANE Select ENSP00000311290.2:p.Pro221=
NM_006261.4:c.663A>C NP_006252.3:p.Pro221=
NM_006261.5:c.663A>C MANE Select NP_006252.4:p.Pro221=
Search 100 bp 5'
Search 100 bp 3'