Canonical Allele Identifier: CA362800539
Gene: GMPR HGNC NCBI

Linked Data

dbSNP Id: rs1042391
gnomAD v4: 6-16290530-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.16290530T>C , CM000668.2:g.16290530T>C GRCh38
NC_000006.11:g.16290761T>C , CM000668.1:g.16290761T>C GRCh37
NC_000006.10:g.16398740T>C NCBI36
NG_013303.1:g.56951T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000259727.5:c.766T>C MANE Select ENSP00000259727.4:p.Phe256Leu
ENST00000259727.4:c.766T>C ENSP00000259727.4:p.Phe256Leu
ENST00000540478.1:n.586T>C
ENST00000543191.5:n.261T>C
ENST00000544145.1:n.120T>C
NM_006877.3:c.766T>C NP_006868.3:p.Phe256Leu
XM_011514508.1:c.909T>C XP_011512810.1:p.Cys303=
XM_011514508.2:c.909T>C XP_011512810.1:p.Cys303=
NM_006877.4:c.766T>C MANE Select NP_006868.3:p.Phe256Leu