Linked Data
dbSNP Id:
rs1043055660
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.121048414A>C , CM000685.2:g.121048414A>C | GRCh38 |
| NC_000023.10:g.120182268A>C , CM000685.1:g.120182268A>C | GRCh37 |
| NC_000023.9:g.120009949A>C | NCBI36 |
| NG_016456.1:g.5807A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328078.3:c.730A>C MANE Select | ENSP00000327589.1:p.Ile244Leu | |
| ENST00000328078.2:c.730A>C | ENSP00000327589.1:p.Ile244Leu | |
| NM_012084.3:c.730A>C | NP_036216.2:p.Ile244Leu | |
| NM_012084.4:c.730A>C MANE Select | NP_036216.2:p.Ile244Leu |