Linked Data
dbSNP Id:
rs2268690
gnomAD v2:
20-57883334-T-C
gnomAD v3:
20-59308279-T-C
gnomAD v4:
20-59308279-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.59308279T>C , CM000682.2:g.59308279T>C | GRCh38 |
| NC_000020.10:g.57883334T>C , CM000682.1:g.57883334T>C | GRCh37 |
| NC_000020.9:g.57316729T>C | NCBI36 |
| NG_008050.1:g.12836T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000337938.7:c.365+6557T>C MANE Select | ENSP00000337128.2:n.365+6557T>C | |
| ENST00000644821.1:c.365+6557T>C | ENSP00000493472.1:n.365+6557T>C | |
| ENST00000671744.1:n.1006+6557T>C | ||
| ENST00000672969.1:c.202+6557T>C | ||
| ENST00000311585.11:c.365+6557T>C | ENSP00000311854.7:n.365+6557T>C | |
| ENST00000337938.6:c.365+6557T>C | ENSP00000337128.2:n.365+6557T>C | |
| ENST00000371025.7:c.365+6557T>C | ENSP00000360064.3:n.365+6557T>C | |
| ENST00000371028.6:c.365+6557T>C | ENSP00000360067.2:n.365+6557T>C | |
| ENST00000395654.3:c.365+6557T>C | ENSP00000379015.3:n.365+6557T>C | |
| NM_001302455.1:c.365+6557T>C | NP_001289384.1:n.365+6557T>C | |
| NM_001302456.1:c.365+6557T>C | NP_001289385.1:n.365+6557T>C | |
| NM_207032.2:c.365+6557T>C | NP_996915.1:n.365+6557T>C | |
| NM_207033.2:c.365+6557T>C | NP_996916.1:n.365+6557T>C | |
| NM_207034.2:c.365+6557T>C | NP_996917.1:n.365+6557T>C | |
| XM_005260312.3:c.365+6557T>C | XP_005260369.1:n.365+6557T>C | |
| XM_005260313.3:c.365+6557T>C | XP_005260370.1:n.365+6557T>C | |
| XM_006723734.2:c.365+6557T>C | XP_006723797.1:n.365+6557T>C | |
| XM_011528655.1:c.365+6557T>C | XP_011526957.1:n.365+6557T>C | |
| XR_936513.1:n.754+6557T>C | ||
| XM_005260312.4:c.365+6557T>C | XP_005260369.1:n.365+6557T>C | |
| XM_005260313.5:c.365+6557T>C | XP_005260370.1:n.365+6557T>C | |
| XM_006723734.3:c.365+6557T>C | XP_006723797.1:n.365+6557T>C | |
| XM_011528655.2:c.365+6557T>C | XP_011526957.1:n.365+6557T>C | |
| XM_024451847.1:c.365+6557T>C | XP_024307615.1:n.365+6557T>C | |
| XM_024451848.1:c.365+6557T>C | XP_024307616.1:n.365+6557T>C | |
| XR_002958461.1:n.763+6557T>C | ||
| XR_002958462.1:n.763+6557T>C | ||
| XR_936513.2:n.762+6557T>C | ||
| NM_207034.3:c.365+6557T>C MANE Select | NP_996917.1:n.365+6557T>C | |
| NM_001302455.2:c.365+6557T>C | NP_001289384.1:n.365+6557T>C | |
| NM_001302456.2:c.365+6557T>C | NP_001289385.1:n.365+6557T>C | |
| NM_207032.3:c.365+6557T>C | NP_996915.1:n.365+6557T>C | |
| NM_207033.3:c.365+6557T>C | NP_996916.1:n.365+6557T>C |