Linked Data
dbSNP Id:
rs752678376
ExAC:
7:21639456 T / C
gnomAD v2:
7-21639456-T-C
gnomAD v4:
7-21599838-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21599838T>C , CM000669.2:g.21599838T>C | GRCh38 |
| NC_000007.13:g.21639456T>C , CM000669.1:g.21639456T>C | GRCh37 |
| NC_000007.12:g.21605981T>C | NCBI36 |
| NG_012886.2:g.61624T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.2719T>C MANE Select | ENSP00000475939.1:p.Tyr907His | |
| ENST00000328843.10:c.2719T>C | ENSP00000330671.7:p.Tyr907His | |
| ENST00000409508.7:c.2719T>C | ENSP00000475939.1:p.Tyr907His | |
| ENST00000620169.4:c.2719T>C | ENSP00000481693.1:p.Tyr907His | |
| NM_001277115.1:c.2719T>C | NP_001264044.1:p.Tyr907His | |
| NM_001277115.2:c.2719T>C MANE Select | NP_001264044.1:p.Tyr907His |