MyVariant.info:
GRCh37
chr1:g.152083325A>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152110849A>G , CM000663.2:g.152110849A>G | GRCh38 |
| NC_000001.10:g.152083325A>G , CM000663.1:g.152083325A>G | GRCh37 |
| NC_000001.9:g.150349949A>G | NCBI36 |
| NG_052960.1:g.9606T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614923.2:c.2368T>C MANE Select | ENSP00000480484.1:p.Leu790= | |
| ENST00000368804.5:c.2368T>C | ENSP00000357794.1:p.Leu790= | |
| ENST00000614923.1:c.2368T>C | ENSP00000480484.1:p.Leu790= | |
| NM_007113.3:c.2368T>C | NP_009044.2:p.Leu790= | |
| NM_007113.4:c.2368T>C MANE Select | NP_009044.2:p.Leu790= |