Linked Data
dbSNP Id:
rs1292080983
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94401601G>C , CM000669.2:g.94401601G>C | GRCh38 |
| NC_000007.13:g.94030913G>C , CM000669.1:g.94030913G>C | GRCh37 |
| NC_000007.12:g.93868849G>C | NCBI36 |
| NG_007405.1:g.12041G>C , LRG_2:g.12041G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.260G>C MANE Select | ENSP00000297268.6:p.Gly87Ala | |
| ENST00000297268.10:c.260G>C | ENSP00000297268.6:p.Gly87Ala | |
| ENST00000620463.1:c.254G>C | ENSP00000477719.1:p.Gly85Ala | |
| NM_000089.3:c.260G>C , LRG_2t1:c.260G>C | NP_000080.2:p.Gly87Ala | |
| NM_000089.4:c.260G>C MANE Select | NP_000080.2:p.Gly87Ala |