Canonical Allele Identifier: CA3645013
Gene: GMPR HGNC NCBI

Linked Data

dbSNP Id: rs767321984
gnomAD v2: 6-16290763-T-G
gnomAD v3: 6-16290532-T-G
gnomAD v4: 6-16290532-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.16290532T>G , CM000668.2:g.16290532T>G GRCh38
NC_000006.11:g.16290763T>G , CM000668.1:g.16290763T>G GRCh37
NC_000006.10:g.16398742T>G NCBI36
NG_013303.1:g.56953T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259727.5:c.768T>G MANE Select ENSP00000259727.4:p.Phe256Leu
ENST00000259727.4:c.768T>G ENSP00000259727.4:p.Phe256Leu
ENST00000540478.1:n.588T>G
ENST00000543191.5:n.263T>G
ENST00000544145.1:n.122T>G
NM_006877.3:c.768T>G NP_006868.3:p.Phe256Leu
XM_011514508.1:c.911T>G XP_011512810.1:p.Leu304Trp
XM_011514508.2:c.911T>G XP_011512810.1:p.Leu304Trp
NM_006877.4:c.768T>G MANE Select NP_006868.3:p.Phe256Leu