Canonical Allele Identifier: CA7902861

Linked Data

dbSNP Id: rs369075574

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281283C>T , CM000678.2:g.11281283C>T GRCh38
NC_000016.9:g.11375140C>T , CM000678.1:g.11375140C>T GRCh37
NC_000016.8:g.11282641C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000312511.4:c.-45G>A (PRM1) MANE Select ENSP00000310515.3:n.-45G>A
ENST00000649869.1:n.152+31505C>T (RMI2)
ENST00000312511.3:c.-45G>A (PRM1) ENSP00000310515.3:n.-45G>A
ENST00000572173.1:c.-515-13933C>T (RMI2) ENSP00000461206.1:n.-515-13933C>T
ENST00000573910.1:n.160+31505C>T (RMI2)
NM_002761.2:c.-45G>A (PRM1) NP_002752.1:n.-45G>A
XR_933070.1:n.733+31505C>T
XR_933070.3:n.876+31505C>T
NM_002761.3:c.-45G>A (PRM1) MANE Select NP_002752.1:n.-45G>A