Linked Data
MyVariant Identifiers:
chr14:g.91739191A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272847A>C , CM000676.2:g.91272847A>C | GRCh38 |
| NC_000014.8:g.91739191A>C , CM000676.1:g.91739191A>C | GRCh37 |
| NC_000014.7:g.90808944A>C | NCBI36 |
| NG_033118.1:g.149998T>G | |
| NG_033118.2:g.149998T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.5865T>G MANE Select | ENSP00000374507.6:p.Pro1955= | |
| ENST00000331194.8:c.1299T>G | ENSP00000330332.8:p.Pro433= | |
| ENST00000389857.10:c.5865T>G | ENSP00000374507.6:p.Pro1955= | |
| ENST00000556726.5:c.2093T>G | ||
| NM_001080414.3:c.5865T>G | NP_001073883.2:p.Pro1955= | |
| XM_011536796.1:c.5757T>G | XP_011535098.1:p.Pro1919= | |
| XM_011536796.2:c.5757T>G | XP_011535098.1:p.Pro1919= | |
| XM_017021336.1:c.2946T>G | XP_016876825.1:p.Pro982= | |
| NM_001080414.4:c.5865T>G MANE Select | NP_001073883.2:p.Pro1955= |