Linked Data
dbSNP Id:
rs777507435
ExAC:
6:32149273 A / T
gnomAD v2:
6-32149273-A-T
gnomAD v4:
6-32181496-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32181496A>T , CM000668.2:g.32181496A>T | GRCh38 |
| NC_000006.11:g.32149273A>T , CM000668.1:g.32149273A>T | GRCh37 |
| NC_000006.10:g.32257251A>T | NCBI36 |
| NG_029868.1:g.7827T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375076.9:c.992-19T>A MANE Select | ENSP00000364217.4:n.992-19T>A | |
| ENST00000375055.6:c.*29+28T>A | ENSP00000364195.2:n.*29+28T>A | |
| ENST00000375065.6:c.179-19T>A | ENSP00000364206.6:n.179-19T>A | |
| ENST00000375067.7:c.837-19T>A | ENSP00000364208.3:n.837-19T>A | |
| ENST00000375069.7:c.1040-19T>A | ENSP00000364210.4:n.1040-19T>A | |
| ENST00000375070.7:c.662-19T>A | ENSP00000364211.4:n.662-19T>A | |
| ENST00000375076.8:c.992-19T>A | ENSP00000364217.4:n.992-19T>A | |
| ENST00000438221.6:c.*29+28T>A | ENSP00000387887.2:n.*29+28T>A | |
| ENST00000469940.5:n.140T>A | ||
| ENST00000473619.5:n.534-19T>A | ||
| ENST00000484849.5:n.1199-19T>A | ||
| ENST00000488669.5:n.615+28T>A | ||
| ENST00000620802.4:c.283-63T>A | ENSP00000484081.1:n.283-63T>A | |
| NM_001136.4:c.992-19T>A | NP_001127.1:n.992-19T>A | |
| NM_001206929.1:c.1040-19T>A | NP_001193858.1:n.1040-19T>A | |
| NM_001206932.1:c.950-19T>A | NP_001193861.1:n.950-19T>A | |
| NM_001206934.1:c.*29+28T>A | NP_001193863.1:n.*29+28T>A | |
| NM_001206936.1:c.1021+28T>A | NP_001193865.1:n.1021+28T>A | |
| NM_001206940.1:c.*29+28T>A | NP_001193869.1:n.*29+28T>A | |
| NM_001206954.1:c.931+28T>A | NP_001193883.1:n.931+28T>A | |
| NM_001206966.1:c.*29+28T>A | NP_001193895.1:n.*29+28T>A | |
| NM_172197.2:c.837-19T>A | NP_751947.1:n.837-19T>A | |
| NR_038190.1:n.1275-19T>A | ||
| XM_017010328.2:c.1072+28T>A | XP_016865817.1:n.1072+28T>A | |
| XR_001743189.2:n.1056-19T>A | ||
| XR_001743190.2:n.1008-19T>A | ||
| NM_001136.5:c.992-19T>A MANE Select | NP_001127.1:n.992-19T>A | |
| NM_001206932.2:c.950-19T>A | NP_001193861.1:n.950-19T>A | |
| NM_001206936.2:c.1021+28T>A | NP_001193865.1:n.1021+28T>A | |
| NM_001206940.2:c.*29+28T>A | NP_001193869.1:n.*29+28T>A | |
| NM_001206954.2:c.931+28T>A | NP_001193883.1:n.931+28T>A | |
| NM_001206966.2:c.*29+28T>A | NP_001193895.1:n.*29+28T>A | |
| NM_172197.3:c.837-19T>A | NP_751947.1:n.837-19T>A | |
| NR_038190.2:n.1206-19T>A | ||
| NM_001206929.2:c.1040-19T>A | NP_001193858.1:n.1040-19T>A | |
| NM_001206934.2:c.*29+28T>A | NP_001193863.1:n.*29+28T>A |