Canonical Allele Identifier: CA2207531652

Gene: PRM1 RMI2

Linked Data

• dbSNP Id: rs373551842
• gnomAD v3: 16-11281241-T-G
• gnomAD v4: 16-11281241-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281241T>G , CM000678.2:g.11281241T>G	GRCh38
NC_000016.9:g.11375098T>G , CM000678.1:g.11375098T>G	GRCh37
NC_000016.8:g.11282599T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000312511.4:c.-3A>C (PRM1) MANE Select	ENSP00000310515.3:n.-3A>C
ENST00000649869.1:n.152+31463T>G (RMI2)
ENST00000312511.3:c.-3A>C (PRM1)	ENSP00000310515.3:n.-3A>C
ENST00000572173.1:c.-515-13975T>G (RMI2)	ENSP00000461206.1:n.-515-13975T>G
ENST00000573910.1:n.160+31463T>G (RMI2)
NM_002761.2:c.-3A>C (PRM1)	NP_002752.1:n.-3A>C
XR_933070.1:n.733+31463T>G
XR_933070.3:n.876+31463T>G
NM_002761.3:c.-3A>C (PRM1) MANE Select	NP_002752.1:n.-3A>C