Linked Data
dbSNP Id:
rs770884481
ExAC:
8:11607624 C / G
gnomAD v2:
8-11607624-C-G
gnomAD v4:
8-11750115-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.11750115C>G , CM000670.2:g.11750115C>G | GRCh38 |
| NC_000008.10:g.11607624C>G , CM000670.1:g.11607624C>G | GRCh37 |
| NC_000008.9:g.11645033C>G | NCBI36 |
| NG_008177.2:g.78197C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622443.3:c.788C>G | ENSP00000482268.2:p.Ala263Gly | |
| ENST00000532059.6:c.791C>G MANE Select | ENSP00000435712.1:p.Ala264Gly | |
| ENST00000335135.8:c.788C>G | ENSP00000334458.4:p.Ala263Gly | |
| ENST00000526716.5:c.170C>G | ENSP00000435347.1:p.Ala57Gly | |
| ENST00000528712.5:c.170C>G | ENSP00000435043.1:p.Ala57Gly | |
| ENST00000532059.5:c.791C>G | ENSP00000435712.1:p.Ala264Gly | |
| ENST00000622443.2:c.785C>G | ENSP00000482268.1:p.Ala262Gly | |
| NM_001308093.1:c.791C>G | NP_001295022.1:p.Ala264Gly | |
| NM_001308094.1:c.170C>G | NP_001295023.1:p.Ala57Gly | |
| NM_002052.3:c.788C>G | NP_002043.2:p.Ala263Gly | |
| NM_002052.4:c.788C>G | NP_002043.2:p.Ala263Gly | |
| XM_005272385.3:c.791C>G | XP_005272442.1:p.Ala264Gly | |
| XM_005272386.1:c.791C>G | XP_005272443.1:p.Ala264Gly | |
| XM_006716248.1:c.791C>G | XP_006716311.1:p.Ala264Gly | |
| XM_011543817.1:c.791C>G | XP_011542119.1:p.Ala264Gly | |
| XM_011543818.1:c.791C>G | XP_011542120.1:p.Ala264Gly | |
| XM_005272385.4:c.791C>G | XP_005272442.1:p.Ala264Gly | |
| XM_011543817.3:c.791C>G | XP_011542119.1:p.Ala264Gly | |
| XM_011543818.2:c.791C>G | XP_011542120.1:p.Ala264Gly | |
| XM_017013312.2:c.791C>G | XP_016868801.1:p.Ala264Gly | |
| NM_001308093.3:c.791C>G MANE Select | NP_001295022.1:p.Ala264Gly | |
| NM_001308094.2:c.170C>G | NP_001295023.1:p.Ala57Gly | |
| NM_001374273.1:c.170C>G | NP_001361202.1:p.Ala57Gly | |
| NM_001374274.1:c.165+1030C>G | NP_001361203.1:n.165+1030C>G | |
| NM_002052.5:c.788C>G | NP_002043.2:p.Ala263Gly |