Linked Data
dbSNP Id:
rs377201195
ExAC:
12:52309036 G / A
gnomAD v2:
12-52309036-G-A
gnomAD v3:
12-51915252-G-A
gnomAD v4:
12-51915252-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51915252G>A , CM000674.2:g.51915252G>A | GRCh38 |
| NC_000012.11:g.52309036G>A , CM000674.1:g.52309036G>A | GRCh37 |
| NC_000012.10:g.50595303G>A | NCBI36 |
| NG_009549.1:g.12835G>A , LRG_543:g.12835G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000547400.6:c.530G>A | ENSP00000446724.2:p.Arg177His | |
| ENST00000551576.6:c.800G>A | ENSP00000455848.2:p.Arg267His | |
| ENST00000552678.2:c.800G>A | ENSP00000457394.2:p.Arg267His | |
| ENST00000388922.9:c.800G>A MANE Select | ENSP00000373574.4:p.Arg267His | |
| ENST00000388922.8:c.800G>A | ENSP00000373574.4:p.Arg267His | |
| ENST00000419526.6:c.278G>A | ENSP00000392492.2:p.Arg93His | |
| ENST00000550683.5:c.842G>A | ENSP00000447884.1:p.Arg281His | |
| NM_000020.2:c.800G>A , LRG_543t1:c.800G>A | NP_000011.2:p.Arg267His | |
| NM_001077401.1:c.800G>A | NP_001070869.1:p.Arg267His | |
| XM_005269235.2:c.800G>A | XP_005269292.1:p.Arg267His | |
| XM_011539008.1:c.530G>A | XP_011537310.1:p.Arg177His | |
| XM_024449279.1:c.11G>A | XP_024305047.1:p.Arg4His | |
| NM_000020.3:c.800G>A MANE Select | NP_000011.2:p.Arg267His | |
| NM_001077401.2:c.800G>A | NP_001070869.1:p.Arg267His |