Canonical Allele Identifier: CA7902847
Gene: PRM1 HGNC NCBI
RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs369840329
ExAC: 16:11375096 G / A
gnomAD v2: 16-11375096-G-A
gnomAD v3: 16-11281239-G-A
gnomAD v4: 16-11281239-G-A
MyVariant Identifiers: chr16:g.11375096G>A (hg19) chr16:g.11281239G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281239G>A , CM000678.2:g.11281239G>A GRCh38
NC_000016.9:g.11375096G>A , CM000678.1:g.11375096G>A GRCh37
NC_000016.8:g.11282597G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000312511.4:c.-1C>T (PRM1) MANE Select ENSP00000310515.3:n.-1C>T
ENST00000649869.1:n.152+31461G>A (RMI2)
ENST00000312511.3:c.-1C>T (PRM1) ENSP00000310515.3:n.-1C>T
ENST00000572173.1:c.-515-13977G>A (RMI2) ENSP00000461206.1:n.-515-13977G>A
ENST00000573910.1:n.160+31461G>A (RMI2)
NM_002761.2:c.-1C>T (PRM1) NP_002752.1:n.-1C>T
XR_933070.1:n.733+31461G>A
XR_933070.3:n.876+31461G>A
NM_002761.3:c.-1C>T (PRM1) MANE Select NP_002752.1:n.-1C>T
Search 100 bp 5'
Search 100 bp 3'