Canonical Allele Identifier: CA7796423
Community Standard Title: NC_000016.10:g.805743G>A
Gene: PRR25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.805743G>A , CM000678.2:g.805743G>A GRCh38
NC_000016.9:g.855743G>A , CM000678.1:g.855743G>A GRCh37
NC_000016.8:g.795744G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001013638.1:c.301G>A NP_001013660.1:p.Ala101Thr
ENST00000301698.1:c.301G>A ENSP00000301698.1:p.Ala101Thr