Linked Data
MyVariant Identifiers:
chr17:g.72915755C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74919660C>T , CM000679.2:g.74919660C>T | GRCh38 |
| NC_000017.10:g.72915755C>T , CM000679.1:g.72915755C>T | GRCh37 |
| NC_000017.9:g.70427350C>T | NCBI36 |
| NG_007882.1:g.8597G>A | |
| NG_033062.1:g.386C>T | |
| NG_007882.2:g.8604G>A | |
| NG_033062.2:g.386C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614341.5:c.1176G>A MANE Select | ENSP00000480279.1:p.Leu392= | |
| ENST00000579243.1:c.*775G>A | ENSP00000462568.1:n.*775G>A | |
| ENST00000614341.4:c.1176G>A | ENSP00000480279.1:p.Leu392= | |
| NM_001282489.2:c.867G>A | NP_001269418.1:p.Leu289= | |
| NM_173477.4:c.1176G>A | NP_775748.2:p.Leu392= | |
| XM_011524296.1:c.867G>A | XP_011522598.1:p.Leu289= | |
| XM_011524296.2:c.867G>A | XP_011522598.1:p.Leu289= | |
| NM_173477.5:c.1176G>A MANE Select | NP_775748.2:p.Leu392= | |
| NM_001282489.3:c.867G>A | NP_001269418.1:p.Leu289= |