Linked Data
gnomAD v4:
14-75003463-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75003463T>C , CM000676.2:g.75003463T>C | GRCh38 |
| NC_000014.8:g.75470166T>C , CM000676.1:g.75470166T>C | GRCh37 |
| NC_000014.7:g.74539919T>C | NCBI36 |
| NG_013333.1:g.5555T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266126.10:c.284+68T>C MANE Select | ENSP00000266126.5:n.284+68T>C | |
| ENST00000266126.9:c.284+68T>C | ENSP00000266126.5:n.284+68T>C | |
| ENST00000553401.5:c.257+68T>C | ENSP00000451681.1:n.257+68T>C | |
| ENST00000553539.1:n.492T>C | ||
| ENST00000555522.1:n.342+68T>C | ||
| ENST00000556028.5:c.284+68T>C | ENSP00000452311.1:n.284+68T>C | |
| NM_014239.3:c.284+68T>C | NP_055054.1:n.284+68T>C | |
| NM_014239.4:c.284+68T>C MANE Select | NP_055054.1:n.284+68T>C |