Canonical Allele Identifier: CA7902792
Gene: PRM1 HGNC NCBI
RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs756199235
ExAC: 16:11374882 G / A
gnomAD v2: 16-11374882-G-A
COSMIC: COSM6195124
MyVariant Identifiers: chr16:g.11374882G>A (hg19) chr16:g.11281025G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281025G>A , CM000678.2:g.11281025G>A GRCh38
NC_000016.9:g.11374882G>A , CM000678.1:g.11374882G>A GRCh37
NC_000016.8:g.11282383G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000312511.4:c.123C>T (PRM1) MANE Select ENSP00000310515.3:p.Arg41=
ENST00000649869.1:n.152+31247G>A (RMI2)
ENST00000312511.3:c.123C>T (PRM1) ENSP00000310515.3:p.Arg41=
ENST00000572173.1:c.-515-14191G>A (RMI2) ENSP00000461206.1:n.-515-14191G>A
ENST00000573910.1:n.160+31247G>A (RMI2)
NM_002761.2:c.123C>T (PRM1) NP_002752.1:p.Arg41=
XR_933070.1:n.733+31247G>A
XR_933070.3:n.876+31247G>A
NM_002761.3:c.123C>T (PRM1) MANE Select NP_002752.1:p.Arg41=
Search 100 bp 5'
Search 100 bp 3'