Linked Data
dbSNP Id:
rs761348826
ExAC:
12:54677755 T / A
gnomAD v2:
12-54677755-T-A
gnomAD v3:
12-54283971-T-A
gnomAD v4:
12-54283971-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.54283971T>A , CM000674.2:g.54283971T>A | GRCh38 |
| NC_000012.11:g.54677755T>A , CM000674.1:g.54677755T>A | GRCh37 |
| NC_000012.10:g.52964022T>A | NCBI36 |
| NG_033830.1:g.8268T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340913.11:c.1063+4T>A MANE Select | ENSP00000341826.7:n.1063+4T>A | |
| ENST00000550482.2:c.907+4T>A | ENSP00000446486.2:n.907+4T>A | |
| ENST00000676572.1:c.289+4T>A | ||
| ENST00000676725.1:n.1237+4T>A | ||
| ENST00000676794.1:c.82+4T>A | ENSP00000504819.1:n.82+4T>A | |
| ENST00000676886.1:c.85-287T>A | ||
| ENST00000677191.1:c.403+4T>A | ||
| ENST00000677210.1:c.1063+4T>A | ENSP00000503610.1:n.1063+4T>A | |
| ENST00000677220.1:c.132+2469T>A | ENSP00000502987.1:n.132+2469T>A | |
| ENST00000677249.1:c.904+4T>A | ENSP00000503649.1:n.904+4T>A | |
| ENST00000677375.1:c.907+4T>A | ENSP00000503651.1:n.907+4T>A | |
| ENST00000677385.1:c.*1253T>A | ENSP00000502985.1:n.*1253T>A | |
| ENST00000677778.1:c.75+1097T>A | ||
| ENST00000677840.1:c.156+4T>A | ||
| ENST00000678077.1:c.772+4T>A | ENSP00000504814.1:n.772+4T>A | |
| ENST00000678212.1:c.251+4T>A | ||
| ENST00000678365.1:n.49-2691T>A | ||
| ENST00000678412.1:c.157-287T>A | ||
| ENST00000678418.1:n.1259+4T>A | ||
| ENST00000678448.1:c.255+4T>A | ENSP00000503619.1:n.255+4T>A | |
| ENST00000678456.1:c.76-287T>A | ||
| ENST00000678970.1:c.232+4T>A | ||
| ENST00000679026.1:c.156+4T>A | ||
| ENST00000679079.1:c.157-578T>A | ||
| ENST00000679228.1:n.1258+4T>A | ||
| ENST00000679273.1:c.243+4T>A | ENSP00000504626.1:n.243+4T>A | |
| ENST00000679344.1:c.264+4T>A | ||
| ENST00000330752.12:c.868+4T>A | ENSP00000333504.8:n.868+4T>A | |
| ENST00000340913.10:c.1063+4T>A | ENSP00000341826.6:n.1063+4T>A | |
| ENST00000546500.5:c.907+4T>A | ENSP00000448617.1:n.907+4T>A | |
| ENST00000547276.5:c.748+4T>A | ENSP00000447260.1:n.748+4T>A | |
| ENST00000547566.5:c.907+4T>A | ENSP00000449913.1:n.907+4T>A | |
| ENST00000550482.1:c.520+4T>A | ENSP00000446486.1:n.520+4T>A | |
| ENST00000551679.1:n.245+4T>A | ||
| NM_002136.2:c.907+4T>A | NP_002127.1:n.907+4T>A | |
| NM_031157.2:c.1063+4T>A | NP_112420.1:n.1063+4T>A | |
| XM_005268826.1:c.1063+4T>A | XP_005268883.1:n.1063+4T>A | |
| XR_245923.1:n.1175+4T>A | ||
| XR_245924.1:n.1019+4T>A | ||
| NM_002136.3:c.907+4T>A | NP_002127.1:n.907+4T>A | |
| NM_031157.3:c.1063+4T>A | NP_112420.1:n.1063+4T>A | |
| NR_135167.1:n.1025+4T>A | ||
| XM_005268826.2:c.1063+4T>A | XP_005268883.1:n.1063+4T>A | |
| XR_245923.2:n.1135+4T>A | ||
| NM_002136.4:c.907+4T>A | NP_002127.1:n.907+4T>A | |
| NM_031157.4:c.1063+4T>A MANE Select | NP_112420.1:n.1063+4T>A | |
| NR_135167.2:n.989+4T>A |