Linked Data
gnomAD v4:
1-119421836-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119421836T>C , CM000663.2:g.119421836T>C | GRCh38 |
| NC_000001.10:g.119964459T>C , CM000663.1:g.119964459T>C | GRCh37 |
| NC_000001.9:g.119765982T>C | NCBI36 |
| NG_013349.1:g.11906T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369416.4:c.335T>C MANE Select | ENSP00000358424.3:p.Val112Ala | |
| ENST00000369416.3:c.335T>C | ENSP00000358424.3:p.Val112Ala | |
| ENST00000433745.5:c.335T>C | ENSP00000388292.1:p.Val112Ala | |
| ENST00000448448.2:n.279T>C | ||
| ENST00000543831.5:c.335T>C | ENSP00000445122.1:p.Val112Ala | |
| NM_000198.3:c.335T>C | NP_000189.1:p.Val112Ala | |
| NM_001166120.1:c.335T>C | NP_001159592.1:p.Val112Ala | |
| NM_000198.4:c.335T>C MANE Select | NP_000189.1:p.Val112Ala | |
| NM_001166120.2:c.335T>C | NP_001159592.1:p.Val112Ala |