Linked Data
MyVariant Identifiers:
chr1:g.16458631C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.16132136C>G , CM000663.2:g.16132136C>G | GRCh38 |
| NC_000001.10:g.16458631C>G , CM000663.1:g.16458631C>G | GRCh37 |
| NC_000001.9:g.16331218C>G | NCBI36 |
| NG_021396.1:g.28952G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000358432.8:c.2253G>C MANE Select | ENSP00000351209.5:p.Leu751= | |
| ENST00000358432.7:c.2253G>C | ENSP00000351209.5:p.Leu751= | |
| NM_004431.3:c.2253G>C | NP_004422.2:p.Leu751= | |
| NM_001329090.1:c.2091G>C | NP_001316019.1:p.Leu697= | |
| NM_004431.4:c.2253G>C | NP_004422.2:p.Leu751= | |
| NM_004431.5:c.2253G>C MANE Select | NP_004422.2:p.Leu751= | |
| NM_001329090.2:c.2091G>C | NP_001316019.1:p.Leu697= |