Canonical Allele Identifier: CA14677905
Gene: PRMT1 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.49685899G>A
GRCh37 chr19:g.50189156G>A
gnomAD v2:
19:50189156 G / A
gnomAD v3:
19:49685899 G / A
gnomAD v4:
chr19-49685899-G-A
Joint Max Group AF 0.3284364 (NFE)
Genomes Max Group AF 0.31888532 (NFE)
Exomes Max Group AF 0.32886513 (NFE)
dbSNP:
10415880
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49685899G>A , CM000681.2:g.49685899G>A GRCh38
NC_000019.9:g.50189156G>A , CM000681.1:g.50189156G>A GRCh37
NC_000019.8:g.54880968G>A NCBI36
NG_031846.1:g.13748G>A
NG_050570.1:g.22G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000454376.7:c.760-194G>A MANE Select ENSP00000406162.2:n.760-194G>A
ENST00000391851.8:c.706-194G>A ENSP00000375724.4:n.706-194G>A
ENST00000454376.6:c.760-194G>A ENSP00000406162.2:n.760-194G>A
ENST00000528126.1:n.176G>A
ENST00000530361.5:n.336-194G>A
ENST00000532489.5:c.622-194G>A ENSP00000433556.1:n.622-194G>A
ENST00000610806.4:c.502-194G>A ENSP00000484505.1:n.502-194G>A
NM_001207042.2:c.502-194G>A NP_001193971.1:n.502-194G>A
NM_001536.5:c.760-194G>A NP_001527.3:n.760-194G>A
NM_198318.4:c.706-194G>A NP_938074.2:n.706-194G>A
NR_033397.4:n.1007-194G>A
XM_005258842.1:c.673-194G>A XP_005258899.1:n.673-194G>A
XM_005258844.3:c.*667G>A XP_005258901.1:n.*667G>A
XM_011526892.1:c.673-194G>A XP_011525194.1:n.673-194G>A
XM_017026734.1:c.688-194G>A XP_016882223.1:n.688-194G>A
XM_017026735.1:c.688-194G>A XP_016882224.1:n.688-194G>A
XM_017026736.1:c.673-194G>A XP_016882225.1:n.673-194G>A
NM_001207042.3:c.502-194G>A NP_001193971.1:n.502-194G>A
NM_001536.6:c.760-194G>A MANE Select NP_001527.3:n.760-194G>A
NM_198318.5:c.706-194G>A NP_938074.2:n.706-194G>A
NR_033397.5:n.888-194G>A
Search 100 bp 5'
Search 100 bp 3'