Linked Data
MyVariant Identifiers:
chr3:g.119132942A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119414095A>T , CM000665.2:g.119414095A>T | GRCh38 |
| NC_000003.11:g.119132942A>T , CM000665.1:g.119132942A>T | GRCh37 |
| NC_000003.10:g.120615632A>T | NCBI36 |
| NG_007665.2:g.124723A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.2166A>T MANE Select | ENSP00000264245.4:p.Pro722= | |
| ENST00000264245.8:c.2166A>T | ENSP00000264245.4:p.Pro722= | |
| NM_020754.3:c.2166A>T | NP_065805.2:p.Pro722= | |
| XM_005247671.3:c.2073A>T | XP_005247728.1:p.Pro691= | |
| XM_006713714.2:c.2106A>T | XP_006713777.1:p.Pro702= | |
| XM_006713714.3:c.2106A>T | XP_006713777.1:p.Pro702= | |
| XM_017006955.1:c.1674A>T | XP_016862444.1:p.Pro558= | |
| NM_020754.4:c.2166A>T MANE Select | NP_065805.2:p.Pro722= |