Linked Data
dbSNP Id:
rs988103378
gnomAD v2:
1-45974068-T-C
gnomAD v3:
1-45508396-T-C
gnomAD v4:
1-45508396-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45508396T>C , CM000663.2:g.45508396T>C | GRCh38 |
| NC_000001.10:g.45974068T>C , CM000663.1:g.45974068T>C | GRCh37 |
| NC_000001.9:g.45746655T>C | NCBI36 |
| NG_013378.1:g.13213T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000401061.9:c.429+32T>C MANE Select | ENSP00000383840.4:n.429+32T>C | |
| ENST00000401061.8:c.429+32T>C | ENSP00000383840.4:n.429+32T>C | |
| ENST00000616135.1:c.258+32T>C | ENSP00000478859.1:n.258+32T>C | |
| NM_015506.2:c.429+32T>C | NP_056321.2:n.429+32T>C | |
| XM_005270724.3:c.234+32T>C | XP_005270781.1:n.234+32T>C | |
| XM_011541204.1:c.258+32T>C | XP_011539506.1:n.258+32T>C | |
| NM_001330540.1:c.258+32T>C | NP_001317469.1:n.258+32T>C | |
| XM_005270724.5:c.234+32T>C | XP_005270781.1:n.234+32T>C | |
| NM_015506.3:c.429+32T>C MANE Select | NP_056321.2:n.429+32T>C | |
| NM_001330540.2:c.258+32T>C | NP_001317469.1:n.258+32T>C |