Linked Data
dbSNP Id:
rs774390535
ExAC:
2:203332296 T / C
gnomAD v2:
2-203332296-T-C
gnomAD v3:
2-202467573-T-C
gnomAD v4:
2-202467573-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202467573T>C , CM000664.2:g.202467573T>C | GRCh38 |
| NC_000002.11:g.203332296T>C , CM000664.1:g.203332296T>C | GRCh37 |
| NC_000002.10:g.203040541T>C | NCBI36 |
| NG_009363.1:g.96247T>C , LRG_712:g.96247T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.302T>C MANE Select | ENSP00000363708.4:p.Val101Ala | |
| ENST00000638587.1:c.233T>C | ENSP00000491062.1:p.Val78Ala | |
| ENST00000374574.2:c.302T>C | ENSP00000363702.2:p.Val101Ala | |
| ENST00000374580.8:c.302T>C | ENSP00000363708.4:p.Val101Ala | |
| ENST00000479069.1:n.209T>C | ||
| NM_001204.6:c.302T>C , LRG_712t1:c.302T>C | NP_001195.2:p.Val101Ala | |
| XM_011511687.1:c.302T>C | XP_011509989.1:p.Val101Ala | |
| XM_011511688.1:c.302T>C | XP_011509990.1:p.Val101Ala | |
| NM_001204.7:c.302T>C MANE Select | NP_001195.2:p.Val101Ala |