Linked Data
gnomAD v4:
2-240873245-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240873245T>C , CM000664.2:g.240873245T>C | GRCh38 |
| NC_000002.11:g.241812662T>C , CM000664.1:g.241812662T>C | GRCh37 |
| NC_000002.10:g.241461335T>C | NCBI36 |
| NG_008005.1:g.9501T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.595+196T>C MANE Select | ENSP00000302620.3:n.595+196T>C | |
| ENST00000307503.3:c.595+196T>C | ENSP00000302620.3:n.595+196T>C | |
| ENST00000472436.1:n.811T>C | ||
| ENST00000476698.1:n.332+196T>C | ||
| NM_000030.2:c.595+196T>C | NP_000021.1:n.595+196T>C | |
| NM_000030.3:c.595+196T>C MANE Select | NP_000021.1:n.595+196T>C |