Linked Data
dbSNP Id:
rs756743469
ExAC:
9:136594971 A / G
gnomAD v2:
9-136594971-A-G
gnomAD v4:
9-133729849-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133729849A>G , CM000671.2:g.133729849A>G | GRCh38 |
| NC_000009.11:g.136594971A>G , CM000671.1:g.136594971A>G | GRCh37 |
| NC_000009.10:g.135584792A>G | NCBI36 |
| NG_008987.1:g.15107T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000439388.6:c.831T>C MANE Select | ENSP00000403084.1:p.Ala277= | |
| ENST00000298628.6:c.831T>C | ENSP00000298628.5:p.Ala277= | |
| ENST00000371867.5:c.564T>C | ENSP00000360933.1:p.Ala188= | |
| ENST00000371872.8:c.831T>C | ENSP00000360938.4:p.Ala277= | |
| ENST00000422262.6:c.-10T>C | ENSP00000415537.3:n.-10T>C | |
| ENST00000427237.6:c.831T>C | ENSP00000394210.2:p.Ala277= | |
| ENST00000439388.5:c.831T>C | ENSP00000403084.1:p.Ala277= | |
| ENST00000616662.4:c.831T>C | ENSP00000484683.1:p.Ala277= | |
| NM_001134707.1:c.831T>C | NP_001128179.1:p.Ala277= | |
| NM_007101.3:c.831T>C | NP_009032.2:p.Ala277= | |
| XM_006716990.2:c.831T>C | XP_006717053.1:p.Ala277= | |
| XM_011518333.1:c.831T>C | XP_011516635.1:p.Ala277= | |
| XR_929726.1:n.998T>C | ||
| XR_929727.1:n.998T>C | ||
| XR_929728.1:n.998T>C | ||
| XM_017014367.1:c.831T>C | XP_016869856.1:p.Ala277= | |
| XM_017014368.1:c.831T>C | XP_016869857.1:p.Ala277= | |
| XR_001746213.1:n.1127T>C | ||
| XR_001746214.1:n.2310T>C | ||
| XR_001746215.1:n.1129T>C | ||
| XR_001746216.1:n.1127T>C | ||
| XR_001746217.1:n.1127T>C | ||
| XR_001746218.1:n.1127T>C | ||
| XR_929726.2:n.998T>C | ||
| NM_001134707.2:c.831T>C MANE Select | NP_001128179.1:p.Ala277= | |
| NM_007101.4:c.831T>C | NP_009032.2:p.Ala277= |