Canonical Allele Identifier: CA3587554
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs766673446
ExAC: 5:177421115 G / C
gnomAD v2: 5-177421115-G-C
gnomAD v4: 5-177994114-G-C
MyVariant Identifiers: chr5:g.177421115G>C (hg19) chr5:g.177994114G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177994114G>C , CM000667.2:g.177994114G>C GRCh38
NC_000005.9:g.177421115G>C , CM000667.1:g.177421115G>C GRCh37
NC_000005.8:g.177353721G>C NCBI36
NG_015889.1:g.7129C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.334C>G MANE Select ENSP00000311290.2:p.Arg112Gly
NM_006261.4:c.334C>G NP_006252.3:p.Arg112Gly
NM_006261.5:c.334C>G MANE Select NP_006252.4:p.Arg112Gly
Search 100 bp 5'
Search 100 bp 3'