Linked Data
gnomAD v4:
2-218893198-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218893198G>T , CM000664.2:g.218893198G>T | GRCh38 |
| NC_000002.11:g.219757920G>T , CM000664.1:g.219757920G>T | GRCh37 |
| NC_000002.10:g.219466164G>T | NCBI36 |
| NG_012179.1:g.17666G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.1181G>T MANE Select | ENSP00000258411.3:p.Cys394Phe | |
| ENST00000258411.7:c.1181G>T | ENSP00000258411.3:p.Cys394Phe | |
| NM_025216.2:c.1181G>T | NP_079492.2:p.Cys394Phe | |
| XM_011511928.1:c.1130G>T | XP_011510230.1:p.Cys377Phe | |
| XM_011511929.1:c.1085G>T | XP_011510231.1:p.Cys362Phe | |
| XM_011511930.1:c.801G>T | XP_011510232.1:p.Leu267= | |
| XM_011511929.2:c.1085G>T | XP_011510231.1:p.Cys362Phe | |
| NM_025216.3:c.1181G>T MANE Select | NP_079492.2:p.Cys394Phe |