Canonical Allele Identifier: CA2631746302
Gene: PRM1 HGNC NCBI
RMI2 HGNC NCBI

Linked Data

gnomAD v4: 16-11281307-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281307A>G , CM000678.2:g.11281307A>G GRCh38
NC_000016.9:g.11375164A>G , CM000678.1:g.11375164A>G GRCh37
NC_000016.8:g.11282665A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000312511.4:c.-69T>C (PRM1) MANE Select ENSP00000310515.3:n.-69T>C
ENST00000649869.1:n.152+31529A>G (RMI2)
ENST00000312511.3:c.-69T>C (PRM1) ENSP00000310515.3:n.-69T>C
ENST00000572173.1:c.-515-13909A>G (RMI2) ENSP00000461206.1:n.-515-13909A>G
ENST00000573910.1:n.160+31529A>G (RMI2)
NM_002761.2:c.-69T>C (PRM1) NP_002752.1:n.-69T>C
XR_933070.1:n.733+31529A>G
XR_933070.3:n.876+31529A>G
NM_002761.3:c.-69T>C (PRM1) MANE Select NP_002752.1:n.-69T>C
Search 100 bp 5'
Search 100 bp 3'