Linked Data
dbSNP Id:
rs1160259613
gnomAD v2:
11-2187924-G-C
gnomAD v3:
11-2166694-G-C
gnomAD v4:
11-2166694-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2166694G>C , CM000673.2:g.2166694G>C | GRCh38 |
| NC_000011.9:g.2187924G>C , CM000673.1:g.2187924G>C | GRCh37 |
| NC_000011.8:g.2144500G>C | NCBI36 |
| NG_008128.1:g.10112C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000352909.8:c.916C>G MANE Select | ENSP00000325951.4:p.Arg306Gly | |
| ENST00000324155.8:c.*605C>G | ENSP00000325831.3:n.*605C>G | |
| ENST00000333684.9:c.696-145C>G | ENSP00000328814.6:n.696-145C>G | |
| ENST00000352909.7:c.916C>G | ENSP00000325951.3:p.Arg306Gly | |
| ENST00000381168.7:c.*636C>G | ENSP00000370560.3:n.*636C>G | |
| ENST00000381175.5:c.997C>G | ENSP00000370567.1:p.Arg333Gly | |
| ENST00000381178.5:c.1009C>G | ENSP00000370571.1:p.Arg337Gly | |
| ENST00000412076.1:c.136-145C>G | ||
| ENST00000416223.5:c.210C>G | ||
| ENST00000461172.1:n.81C>G | ||
| ENST00000479437.5:n.465C>G | ||
| NM_000360.3:c.916C>G | NP_000351.2:p.Arg306Gly | |
| NM_199292.2:c.1009C>G | NP_954986.2:p.Arg337Gly | |
| NM_199293.2:c.997C>G | NP_954987.2:p.Arg333Gly | |
| XM_011520335.1:c.928C>G | XP_011518637.1:p.Arg310Gly | |
| XM_011520335.2:c.928C>G | XP_011518637.1:p.Arg310Gly | |
| NM_000360.4:c.916C>G MANE Select | NP_000351.2:p.Arg306Gly | |
| NM_199292.3:c.1009C>G | NP_954986.2:p.Arg337Gly | |
| NM_199293.3:c.997C>G | NP_954987.2:p.Arg333Gly |