Linked Data
dbSNP Id:
rs780939353
gnomAD v2:
3-30715568-A-T
gnomAD v3:
3-30674076-A-T
gnomAD v4:
3-30674076-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30674076A>T , CM000665.2:g.30674076A>T | GRCh38 |
| NC_000003.11:g.30715568A>T , CM000665.1:g.30715568A>T | GRCh37 |
| NC_000003.10:g.30690572A>T | NCBI36 |
| NG_007490.1:g.72575A>T , LRG_779:g.72575A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295754.10:c.1255-29A>T MANE Select | ENSP00000295754.5:n.1255-29A>T | |
| ENST00000672866.1:n.2851-29A>T | ||
| ENST00000673203.1:n.104A>T | ||
| ENST00000295754.9:c.1255-29A>T | ENSP00000295754.5:n.1255-29A>T | |
| ENST00000359013.4:c.1330-29A>T | ENSP00000351905.4:n.1330-29A>T | |
| NM_001024847.2:c.1330-29A>T , LRG_779t1:c.1330-29A>T | NP_001020018.1:n.1330-29A>T | |
| NM_003242.5:c.1255-29A>T | NP_003233.4:n.1255-29A>T | |
| XM_011534043.1:c.1282-29A>T | XP_011532345.1:n.1282-29A>T | |
| XM_011534044.1:c.1207-29A>T | XP_011532346.1:n.1207-29A>T | |
| XM_011534045.1:c.1150-29A>T | XP_011532347.1:n.1150-29A>T | |
| XM_011534043.2:c.1282-29A>T | XP_011532345.1:n.1282-29A>T | |
| XM_011534045.3:c.1150-29A>T | XP_011532347.1:n.1150-29A>T | |
| XM_017007106.1:c.1150-29A>T | XP_016862595.1:n.1150-29A>T | |
| NM_003242.6:c.1255-29A>T MANE Select | NP_003233.4:n.1255-29A>T |