Canonical Allele Identifier: CA7902812
Gene: PRM1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs35576928

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281137C>A , CM000678.2:g.11281137C>A GRCh38
NC_000016.9:g.11374994C>A , CM000678.1:g.11374994C>A GRCh37
NC_000016.8:g.11282495C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002761.2:c.102G>T VV NP_002752.1:p.Arg34Ser
XR_933070.1:n.733+31359C>A
XR_933070.3:n.876+31359C>A
NM_002761.3:c.102G>T VV MANE Preferred NP_002752.1:p.Arg34Ser
ENST00000312511.3:c.102G>T ENSP00000310515.3:p.Arg34Ser
ENST00000572173.1:c.-515-14079C>A ENSP00000461206.1:p.=
ENST00000573910.1:n.160+31359C>A