Linked Data
gnomAD v4:
10-104034621-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.104034621T>C , CM000672.2:g.104034621T>C | GRCh38 |
| NC_000010.10:g.105794379T>C , CM000672.1:g.105794379T>C | GRCh37 |
| NC_000010.9:g.105784369T>C | NCBI36 |
| NG_007069.1:g.56260A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369733.8:c.3520A>G | ENSP00000358748.3:p.Ser1174Gly | |
| ENST00000648076.2:c.3766A>G MANE Select | ENSP00000497653.1:p.Ser1256Gly | |
| ENST00000353479.9:c.3766A>G | ENSP00000340937.5:p.Ser1256Gly | |
| ENST00000369733.7:c.3520A>G | ENSP00000358748.3:p.Ser1174Gly | |
| NM_000494.3:c.3766A>G | NP_000485.3:p.Ser1256Gly | |
| NM_000494.4:c.3766A>G MANE Select | NP_000485.3:p.Ser1256Gly |