Linked Data
dbSNP Id:
rs754445822
ExAC:
2:128178893 G / C
gnomAD v2:
2-128178893-G-C
gnomAD v4:
2-127421317-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.127421317G>C , CM000664.2:g.127421317G>C | GRCh38 |
| NC_000002.11:g.128178893G>C , CM000664.1:g.128178893G>C | GRCh37 |
| NC_000002.10:g.127895363G>C | NCBI36 |
| NG_016323.1:g.7898G>C , LRG_599:g.7898G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000234071.8:c.105G>C MANE Select | ENSP00000234071.4:p.Gln35His | |
| ENST00000234071.7:c.105G>C | ENSP00000234071.3:p.Gln35His | |
| ENST00000409048.1:c.105G>C | ENSP00000386679.1:p.Gln35His | |
| ENST00000419985.5:c.71-1G>C | ENSP00000392606.1:n.71-1G>C | |
| ENST00000427769.5:c.105G>C | ENSP00000406295.1:p.Gln35His | |
| ENST00000429925.5:c.105G>C | ENSP00000412697.1:p.Gln35His | |
| ENST00000431364.1:c.71-1G>C | ENSP00000391220.1:n.71-1G>C | |
| ENST00000442644.5:c.105G>C | ENSP00000411241.1:p.Gln35His | |
| ENST00000474030.5:n.188G>C | ||
| NM_000312.3:c.105G>C , LRG_599t1:c.105G>C | NP_000303.1:p.Gln35His | |
| XM_005263715.3:c.288G>C | XP_005263772.1:p.Gln96His | |
| XM_005263716.3:c.168G>C | XP_005263773.1:p.Gln56His | |
| XM_005263717.3:c.168G>C | XP_005263774.1:p.Gln56His | |
| XM_005263717.4:c.168G>C | XP_005263774.1:p.Gln56His | |
| XM_017004505.1:c.349-1G>C | XP_016859994.1:n.349-1G>C | |
| XM_024453002.1:c.349-1G>C | XP_024308770.1:n.349-1G>C | |
| XM_024453003.1:c.288G>C | XP_024308771.1:p.Gln96His | |
| XM_024453004.1:c.288G>C | XP_024308772.1:p.Gln96His | |
| XM_024453005.1:c.168G>C | XP_024308773.1:p.Gln56His | |
| XM_024453006.1:c.105G>C | XP_024308774.1:p.Gln35His | |
| NM_000312.4:c.105G>C MANE Select | NP_000303.1:p.Gln35His | |
| NM_001375602.1:c.288G>C | NP_001362531.1:p.Gln96His | |
| NM_001375603.1:c.168G>C | NP_001362532.1:p.Gln56His | |
| NM_001375604.1:c.168G>C | NP_001362533.1:p.Gln56His | |
| NM_001375605.1:c.105G>C | NP_001362534.1:p.Gln35His | |
| NM_001375606.1:c.168G>C | NP_001362535.1:p.Gln56His | |
| NM_001375607.1:c.190-1G>C | NP_001362536.1:n.190-1G>C | |
| NM_001375608.1:c.105G>C | NP_001362537.1:p.Gln35His | |
| NM_001375609.1:c.81G>C | NP_001362538.1:p.Gln27His | |
| NM_001375610.1:c.99G>C | NP_001362539.1:p.Gln33His | |
| NM_001375611.1:c.105G>C | NP_001362540.1:p.Gln35His | |
| NM_001375613.1:c.105G>C | NP_001362542.1:p.Gln35His |